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- [1] Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variantsGENETICS IN MEDICINE, 2018, 20 (10) : 1175 - 1185Johnston, Jennifer J.论文数: 0 引用数: 0 h-index: 0机构: NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USA Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAvan der Smagt, Jasper J.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USARosenfeld, Jill A.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAPagnamenta, Alistair T.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Natl Inst Hlth Res, Wellcome Ctr Human Genet, Oxford Biomed Res Ctr, Oxford, England NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAAlswaid, Abdulrahman论文数: 0 引用数: 0 h-index: 0机构: King Abdul Aziz Med City, Riyadh, Saudi Arabia NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USABaker, Eva H.论文数: 0 引用数: 0 h-index: 0机构: NIH, Dept Radiol & Imaging Serv, Bldg 10, Bethesda, MD 20892 USA NIH, Clin Ctr, Bldg 10, Bethesda, MD 20892 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USABlair, Edward论文数: 0 引用数: 0 h-index: 0机构: Oxford Univ Hosp NHS Fdn Trust, Oxford Ctr Genom Med, Oxford, England NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USABorck, Guntram论文数: 0 引用数: 0 h-index: 0机构: Univ Ulm, Inst Human Genet, Ulm, Germany NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USABrinkmann, Julia论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp, Inst Human Genet, Magdeburg, Germany NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USACraigen, William论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAVu Chi Dung论文数: 0 引用数: 0 h-index: 0机构: Natl Childrens Hosp, Dept Med Genet & Metab, Rare Dis & Newborn Screening Serv, Hanoi, Vietnam NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAEmrick, Lisa论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Div Neurol & Dev Neurosci, Houston, TX 77030 USA Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAEverman, David B.论文数: 0 引用数: 0 h-index: 0机构: Greenwood Genet Ctr, Greenwood, SC 29646 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAvan Gassen, Koen L.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAGulsuner, Suleyman论文数: 0 引用数: 0 h-index: 0机构: Univ Washington, Div Med Genet, Seattle, WA 98195 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAHarr, Margaret H.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Ctr Appl Genom, Philadelphia, PA 19104 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAJain, Mahim论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA Johns Hopkins Med Inst, Kennedy Krieger Inst, Baltimore, MD 21205 USA Johns Hopkins Med Inst, Dept Pediat, Baltimore, MD 21205 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAKuechler, Alma论文数: 0 引用数: 0 h-index: 0机构: Univ Duisburg Essen, Univ Klinikum Essen, Inst Humangenet, Essen, Germany NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USALeppig, Kathleen A.论文数: 0 引用数: 0 h-index: 0机构: Kaiser Permanente Washington, Genet Serv, Seattle, WA USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAMcDonald-McGinn, Donna M.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Childrens Hosp Philadelphia, Dept Pediat, Philadelphia, PA 19104 USA Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USANgoc Thi Bich Can论文数: 0 引用数: 0 h-index: 0机构: Natl Childrens Hosp, Dept Med Genet & Metab, Rare Dis & Newborn Screening Serv, Hanoi, Vietnam NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAPeleg, Amir论文数: 0 引用数: 0 h-index: 0机构: Carmel Hosp, Inst Human Genet, Haifa, Israel NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USARoeder, Elizabeth R.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Pediat & Mol & Human Genet, San Antonio, TX USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USARogers, R. Curtis论文数: 0 引用数: 0 h-index: 0机构: Greenwood Genet Ctr, Greenwood, SC 29646 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USASagi-Dain, Lena论文数: 0 引用数: 0 h-index: 0机构: Carmel Hosp, Inst Human Genet, Haifa, Israel NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USASapp, Julie C.论文数: 0 引用数: 0 h-index: 0机构: NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USASchaffer, Alejandro A.论文数: 0 引用数: 0 h-index: 0机构: NIH, Computat Biol Branch, Natl Ctr Biotechnol Informat, Bldg 10, Bethesda, MD 20892 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USASchanze, Denny论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp, Inst Human Genet, Magdeburg, Germany NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAStewart, Helen论文数: 0 引用数: 0 h-index: 0机构: Oxford Univ Hosp NHS Fdn Trust, Oxford Ctr Genom Med, Oxford, England NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USATaylor, Jenny C.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Natl Inst Hlth Res, Wellcome Ctr Human Genet, Oxford Biomed Res Ctr, Oxford, England NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAVerbeek, Nienke E.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAWalkiewicz, Magdalena A.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA NIAID, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAZackai, Elaine H.论文数: 0 引用数: 0 h-index: 0机构: Univ Penn, Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Childrens Hosp Philadelphia, Dept Pediat, Philadelphia, PA 19104 USA Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAZweier, Christiane论文数: 0 引用数: 0 h-index: 0机构: Friedrich Alexander Univ Erlangen Nurnberg, Inst Human Genet, Erlangen, Germany NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USAZenker, Martin论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp, Inst Human Genet, Magdeburg, Germany NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USALee, Brendan论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USABiesecker, Leslie G.论文数: 0 引用数: 0 h-index: 0机构: NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USA NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USA
- [2] Noonan syndrome associated with growth hormone deficiency with biallelic LZTR1 variantsGENETICS IN MEDICINE, 2019, 21 (01) : 260 - 260Nakaguma, Marilena论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Unidade Endocrinol Desenvolvimento, Lab Hormonios & Genet Mol LIM42, Hosp Clin,Disciplina Endocrinol,Fac Med, Sao Paulo, Brazil Univ Sao Paulo, Unidade Endocrinol Desenvolvimento, Lab Hormonios & Genet Mol LIM42, Hosp Clin,Disciplina Endocrinol,Fac Med, Sao Paulo, BrazilJorge, Alexander A. L.论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Unidade Endocrinol Genet, Lab Endocrinol Celular & Mol LIM25, Hosp Clin,Disciplina Endocrinol,Fac Med, Sao Paulo, Brazil Univ Sao Paulo, Unidade Endocrinol Desenvolvimento, Lab Hormonios & Genet Mol LIM42, Hosp Clin,Disciplina Endocrinol,Fac Med, Sao Paulo, BrazilArnhold, Ivo J. P.论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Unidade Endocrinol Desenvolvimento, Lab Hormonios & Genet Mol LIM42, Hosp Clin,Disciplina Endocrinol,Fac Med, Sao Paulo, Brazil Univ Sao Paulo, Unidade Endocrinol Desenvolvimento, Lab Hormonios & Genet Mol LIM42, Hosp Clin,Disciplina Endocrinol,Fac Med, Sao Paulo, Brazil
- [3] Noonan syndrome associated with growth hormone deficiency with biallelic LZTR1 variants ResponseGENETICS IN MEDICINE, 2019, 21 (01) : 261 - 261Biesecker, Leslie G.论文数: 0 引用数: 0 h-index: 0机构: NHGRI, NIH, Bethesda, MD 20892 USA NHGRI, NIH, Bethesda, MD 20892 USA
- [4] LZTR1: Genotype Expansion in Noonan SyndromeHORMONE RESEARCH IN PAEDIATRICS, 2020, 92 (04): : 269 - 275Guemes, Maria论文数: 0 引用数: 0 h-index: 0机构: Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat Endocrinol, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain La Princesa Res Inst, Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, SpainMartin-Rivada, Alvaro论文数: 0 引用数: 0 h-index: 0机构: Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat Endocrinol, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, SpainOrtiz-Cabrera, Neimar Valentina论文数: 0 引用数: 0 h-index: 0机构: Hosp Infantil Univ Nino Jesus, Dept Clin Genet, Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, SpainMartos-Moreno, Gabriel Angel论文数: 0 引用数: 0 h-index: 0机构: Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat Endocrinol, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain La Princesa Res Inst, Madrid, Spain Univ Autonoma Madrid, Dept Pediat, Madrid, Spain Inst Salud Carlos III, Ctr Invest Biomed Red Fisiopatol Obesidad & Nutr, Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, SpainPozo-Roman, Jesus论文数: 0 引用数: 0 h-index: 0机构: Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat Endocrinol, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain La Princesa Res Inst, Madrid, Spain Univ Autonoma Madrid, Dept Pediat, Madrid, Spain Inst Salud Carlos III, Ctr Invest Biomed Red Fisiopatol Obesidad & Nutr, Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, SpainArgente, Jesus论文数: 0 引用数: 0 h-index: 0机构: Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat Endocrinol, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain La Princesa Res Inst, Madrid, Spain Univ Autonoma Madrid, Dept Pediat, Madrid, Spain Inst Salud Carlos III, Ctr Invest Biomed Red Fisiopatol Obesidad & Nutr, Madrid, Spain CEIUAM CSI, Food Inst, IMDEA, Madrid, Spain Hosp Infantil Univ Nino Jesus, Dept Pediat, Avda Menendez Pelayo 65, ES-28009 Madrid, Spain
- [5] A novel missense variant in the LZTR1 gene in a patient with an overlapping phenotype of autosomal dominant Noonan Syndrome and SchwannomatosisEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1127 - 1128Calosci, Davide论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, Italy Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, ItalyPassaglia, Lisa论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, Italy Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, ItalyCalo, Annapaola论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Padova, Clin Genet Unit, Padua, Italy Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, ItalyRigon, Chiara论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, Italy Ist Ric Pediat, Fdn Citta Speranza, Padua, Italy Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, ItalyAli, Dario Seif论文数: 0 引用数: 0 h-index: 0机构: AOU Marche, SOSD Genet Med & Coordinamento Malattie Rare, Ancona, Italy Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, ItalyBertolin, Cinzia论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Padova, Clin Genet Unit, Padua, Italy Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, ItalyTrevisson, Eva论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, Italy Univ Hosp Padova, Clin Genet Unit, Padua, Italy Ist Ric Pediat, Fdn Citta Speranza, Padua, Italy Univ Padua, Dept Womens & Childrens Hlth SDB, Padua, Italy
- [6] Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexesHuman Genetics, 2019, 138 : 21 - 35Ikumi Umeki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsTetsuya Niihori论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsTaiki Abe论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsShin-ichiro Kanno论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsNobuhiko Okamoto论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsSeiji Mizuno论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsKenji Kurosawa论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsKeisuke Nagasaki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsMakoto Yoshida论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsHirofumi Ohashi论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsShin-ichi Inoue论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsYoichi Matsubara论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsIkuma Fujiwara论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsShigeo Kure论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsYoko Aoki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical Genetics
- [7] Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1-PPP1CB complexesHUMAN GENETICS, 2019, 138 (01) : 21 - 35Umeki, Ikumi论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, Japan论文数: 引用数: h-index:机构:Abe, Taiki论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanKanno, Shin-ichiro论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Inst Dev Aging & Canc, Div Dynam Proteome Canc & Aging, Sendai, Miyagi, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanOkamoto, Nobuhiko论文数: 0 引用数: 0 h-index: 0机构: Osaka Womens & Childrens Hosp, Dept Med Genet, Izumi, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanMizuno, Seiji论文数: 0 引用数: 0 h-index: 0机构: Aichi Human Serv Ctr, Cent Hosp, Dept Pediat, Kasugai, Aichi, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanKurosawa, Kenji论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Med Genet, Yokohama, Kanagawa, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanNagasaki, Keisuke论文数: 0 引用数: 0 h-index: 0机构: Niigata Univ, Grad Sch Med & Dent Sci, Dept Homeostat Regulat & Dev, Div Pediat, Niigata, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanYoshida, Makoto论文数: 0 引用数: 0 h-index: 0机构: Sano Kosei Gen Hosp, Dept Pediat, Sano, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanOhashi, Hirofumi论文数: 0 引用数: 0 h-index: 0机构: Saitama Childrens Med Ctr, Div Med Genet, Saitama, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanInoue, Shin-ichi论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanMatsubara, Yoichi论文数: 0 引用数: 0 h-index: 0机构: Natl Res Inst Child Hlth & Dev, Tokyo, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanFujiwara, Ikuma论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Grad Sch Med, Dept Pediat Endocrinol & Environm Med, Sendai, Miyagi, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanKure, Shigeo论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Pediat, Sch Med, Sendai, Miyagi, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, JapanAoki, Yoko论文数: 0 引用数: 0 h-index: 0机构: Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, Japan Tohoku Univ, Dept Med Genet, Sch Med, Aoba Ku, 1-1 Seiryomachi, Sendai, Miyagi 9808574, Japan
- [8] Noonan syndrome-associated biallelic LZTR1 mutations cause cardiac hypertrophy and vascular malformations in zebrafishMOLECULAR GENETICS & GENOMIC MEDICINE, 2020, 8 (03):Nakagama, Yu论文数: 0 引用数: 0 h-index: 0机构: Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, Japan Osaka City Univ, Grad Sch Med, Dept Parasitol, Osaka, Japan Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, JapanTakeda, Norihiko论文数: 0 引用数: 0 h-index: 0机构: Univ Tokyo, Grad Sch Med, Dept Cardiovasc Med, Tokyo, Japan Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, Japan论文数: 引用数: h-index:机构:Takeda, Hiroyuki论文数: 0 引用数: 0 h-index: 0机构: Univ Tokyo, Grad Sch Sci, Dept Biol Sci, Tokyo, Japan Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, JapanFurutani, Yoshiyuki论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Dept Pediat Cardiol & Adult Congenital Cardiol, Tokyo, Japan Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, JapanNakanishi, Toshio论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Dept Pediat Cardiol & Adult Congenital Cardiol, Tokyo, Japan Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, JapanSato, Tatsuyuki论文数: 0 引用数: 0 h-index: 0机构: Univ Tokyo, Grad Sch Med, Dept Cardiovasc Med, Tokyo, Japan Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, JapanHirata, Yoichiro论文数: 0 引用数: 0 h-index: 0机构: Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, Japan Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, JapanOka, Akira论文数: 0 引用数: 0 h-index: 0机构: Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, Japan Univ Tokyo, Dept Pediat, Grad Sch Med, Tokyo, Japan论文数: 引用数: h-index:机构:
- [9] Unilateral vestibular schwannoma in a patient with schwannomatosis in the absence of LZTR1 mutationJOURNAL OF NEUROSURGERY, 2016, 125 (06) : 1469 - 1471Mehta, Gautam U.论文数: 0 引用数: 0 h-index: 0机构: NINDS, Surg Neurol Branch, NIH, 10 Ctr Dr,Rm 3D20, Bethesda, MD 20892 USA Univ Virginia Hlth Syst, Dept Neurosurg, Charlottesville, VA USA NINDS, Surg Neurol Branch, NIH, 10 Ctr Dr,Rm 3D20, Bethesda, MD 20892 USAFeldman, Michael J.论文数: 0 引用数: 0 h-index: 0机构: NINDS, Surg Neurol Branch, NIH, 10 Ctr Dr,Rm 3D20, Bethesda, MD 20892 USA NINDS, Surg Neurol Branch, NIH, 10 Ctr Dr,Rm 3D20, Bethesda, MD 20892 USAWang, Herui论文数: 0 引用数: 0 h-index: 0机构: NINDS, Surg Neurol Branch, NIH, 10 Ctr Dr,Rm 3D20, Bethesda, MD 20892 USA NINDS, Surg Neurol Branch, NIH, 10 Ctr Dr,Rm 3D20, Bethesda, MD 20892 USADing, Dale论文数: 0 引用数: 0 h-index: 0机构: Univ Virginia Hlth Syst, Dept Neurosurg, Charlottesville, VA USA NINDS, Surg Neurol Branch, NIH, 10 Ctr Dr,Rm 3D20, Bethesda, MD 20892 USAChittiboina, Prashant论文数: 0 引用数: 0 h-index: 0机构: NINDS, Surg Neurol Branch, NIH, 10 Ctr Dr,Rm 3D20, Bethesda, MD 20892 USA NINDS, Surg Neurol Branch, NIH, 10 Ctr Dr,Rm 3D20, Bethesda, MD 20892 USA
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