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- [21] SEVERE SMARCAL1 NOVEL MUTATION ASSOCIATES WITH A CHROMOSOMAL BREAKAGE PHENOTYPE IN SCHIMKE PATIENTJOURNAL OF CLINICAL IMMUNOLOGY, 2012, 32 : 316 - 316Simon, A. J.论文数: 0 引用数: 0 h-index: 0机构: Sheba Med Ctr, Sheba Canc Res Ctr, Tel Hashomer, Israel Sheba Med Ctr, Sheba Canc Res Ctr, Tel Hashomer, IsraelKorn, D.论文数: 0 引用数: 0 h-index: 0机构: Edmond & Lily Safra Childrens Hosp, Sheba Med Ctr, Dept Pediat, Immunol Unit, Ramat Gan, Israel Sheba Med Ctr, Sheba Canc Res Ctr, Tel Hashomer, IsraelLev, A.论文数: 0 引用数: 0 h-index: 0机构: Edmond & Lily Safra Childrens Hosp, Sheba Med Ctr, Dept Pediat, Immunol Unit, Ramat Gan, Israel Sheba Med Ctr, Sheba Canc Res Ctr, Tel Hashomer, IsraelLerenthal, Y.论文数: 0 引用数: 0 h-index: 0机构: Sheba Med Ctr, Sheba Canc Res Ctr, Tel Hashomer, Israel Sheba Med Ctr, Sheba Canc Res Ctr, Tel Hashomer, IsraelSomech, R.论文数: 0 引用数: 0 h-index: 0机构: Edmond & Lily Safra Childrens Hosp, Sheba Med Ctr, Dept Pediat, Immunol Unit, Ramat Gan, Israel Sheba Med Ctr, Sheba Canc Res Ctr, Tel Hashomer, Israel
- [22] Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora diseaseNEUROGENETICS, 2009, 10 (04) : 319 - 323Traore, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Bamako, Dept Neurosci, Bamako, Mali UCL, Royal Free Hosp, London NW3 2PF, EnglandLandoure, G.论文数: 0 引用数: 0 h-index: 0机构: UCL, Royal Free Hosp, London NW3 2PF, England Univ Bamako, Dept Neurosci, Bamako, Mali Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandMotley, W.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandSangare, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Bamako, Dept Neurosci, Bamako, Mali Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandMeilleur, K.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA NINR, NIH, Bethesda, MD 20892 USA Johns Hopkins Univ, Sch Nursing, Baltimore, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandCoulibaly, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Bamako, Dept Neurosci, Bamako, Mali UCL, Royal Free Hosp, London NW3 2PF, EnglandTraore, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Bamako, Dept Neurosci, Bamako, Mali UCL, Royal Free Hosp, London NW3 2PF, EnglandNiare, B.论文数: 0 引用数: 0 h-index: 0机构: Univ Bamako, Dept Neurosci, Bamako, Mali UCL, Royal Free Hosp, London NW3 2PF, EnglandMochel, F.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA Hop La Pitie Salpetriere, INSERM, U679, Paris, France UCL, Royal Free Hosp, London NW3 2PF, EnglandLa Pean, A.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandVortmeyer, A.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandMani, H.论文数: 0 引用数: 0 h-index: 0机构: NCI, NIH, Bethesda, MD 20892 USA UCL, Royal Free Hosp, London NW3 2PF, EnglandFischbeck, K. H.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, England
- [23] Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora diseaseneurogenetics, 2009, 10 : 319 - 323M. Traoré论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesG. Landouré论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesW. Motley论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesM. Sangaré论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesK. Meilleur论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesS. Coulibaly论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesS. Traoré论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesB. Niaré论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesF. Mochel论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesA. La Pean论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesA. Vortmeyer论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesH. Mani论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of NeurosciencesK. H. Fischbeck论文数: 0 引用数: 0 h-index: 0机构: University of Bamako,Department of Neurosciences
- [24] Correction to: The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotypeJournal of Molecular Medicine, 2021, 99 : 1769 - 1770Luisa Averdunk论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfHeinrich Sticht论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfHarald Surowy论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfHermann‑Josef Lüdecke论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfMargarete Koch‑Hogrebe论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfHessa S. Alsaif论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfKimia Kahrizi论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfHamad Alzaidan论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfBashayer S. Alawam论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfMohamed Tohary论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfCornelia Kraus论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfSabine Endele论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfErin Wadman论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfJulie D. Kaplan论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfStephanie Efthymiou论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfHossein Najmabadi论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfAndré Reis论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfFowzan S. Alkuraya论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital DüsseldorfDagmar Wieczorek论文数: 0 引用数: 0 h-index: 0机构: Heinrich-Heine-University Düsseldorf,Institute of Human Genetics, Medical Faculty and University Hospital Düsseldorf
- [25] A novel homozygous missense mutation in SLURP1 causes Mal de Meleda with an atypical phenotypeEXPERIMENTAL DERMATOLOGY, 2011, 20 (02) : 173 - 173Gruber, R.论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Dept Dermatol & Venereol, A-6020 Innsbruck, Austria Innsbruck Med Univ, Dept Dermatol & Venereol, A-6020 Innsbruck, AustriaHennies, H. C.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Div Dermatogenet, Cologne, Germany Innsbruck Med Univ, Dept Dermatol & Venereol, A-6020 Innsbruck, AustriaRomani, N.论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Dept Dermatol & Venereol, A-6020 Innsbruck, Austria Innsbruck Med Univ, Dept Dermatol & Venereol, A-6020 Innsbruck, AustriaSchmuth, M.论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Dept Dermatol & Venereol, A-6020 Innsbruck, Austria Innsbruck Med Univ, Dept Dermatol & Venereol, A-6020 Innsbruck, Austria
- [26] A Roma founder BIN1 mutation causes a novel phenotype of centronuclear myopathy with rigid spineNEUROLOGY, 2018, 91 (04) : E339 - E348Cabrera-Serrano, Macarena论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, Spain Hosp Univ Virgen del Rocio, Inst Biomed Sevilla IBiS, Seville, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainMavillard, Fabiola论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Virgen del Rocio, Inst Biomed Sevilla IBiS, Seville, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainBiancalana, Valerie论文数: 0 引用数: 0 h-index: 0机构: CHRU, Lab Diagnost Genet, Fac Med, Strasbourg, France IGBMC, Illkirch Graffenstaden, France Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainRivas, Eloy论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Virgen del Rocio, Dept Pathol, Neuropathol Unit, Seville, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainMorar, Bharti论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Harry Perkins Inst Med Res, Nedlands, WA, Australia Univ Western Australia, Med Res Ctr, Nedlands, WA, Australia Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainHernandez-Lain, Aurelio论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ 12 Octubre, Dept Pathol Neuropathol, Res Inst, Madrid, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainOlive, Montse论文数: 0 引用数: 0 h-index: 0机构: Hosp Bellvitge Princeps Espanya, Neuropathol Unit, Dept Pathol, IDIBELL, Barcelona, Spain Hosp Bellvitge Princeps Espanya, Neuromuscular Unit, Dept Neurol, IDIBELL, Barcelona, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainMuelas, Nuria论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Politecn La Fe, Dept Neurol, Valencia, Spain Hosp Univ Politecn La Fe, IIS La Fe, Valencia, Spain Hosp Gen Univ Santa Lucia, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Consulta Enfermedades Neuromusculares, Murcia, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainKhan, Eduardo论文数: 0 引用数: 0 h-index: 0机构: Hosp Gen Univ Santa Lucia, Dept Neurol, Consulta Enfermedades Neuromusculares, Murcia, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainCarvajal, Alejandra论文数: 0 引用数: 0 h-index: 0机构: Hosp Virgen de las Nieves, Dept Neurol, Granada, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainQuiroga, Pablo论文数: 0 引用数: 0 h-index: 0机构: Hosp Torrecardenas, Dept Neurol, Almeria, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainDiaz-Manera, Jordi论文数: 0 引用数: 0 h-index: 0机构: Hosp Gen Univ Santa Lucia, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Consulta Enfermedades Neuromusculares, Murcia, Spain Univ Autonoma Barcelona, Unidad Enfermedades Neuromusculares, Dept Neurol, Hosp Santa Creu & St Pau, Barcelona, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainDavis, Mark论文数: 0 引用数: 0 h-index: 0机构: PathWest Lab Med WA, Dept Diagnost Genom, Perth, WA, Australia Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainAvila, Rainiero论文数: 0 引用数: 0 h-index: 0机构: IGBMC, Illkirch Graffenstaden, France Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainDominguez, Cristina论文数: 0 引用数: 0 h-index: 0机构: Hosp 12 Octubre, Dept Neurol, Madrid, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainRomero, Norma Beatriz论文数: 0 引用数: 0 h-index: 0机构: Grp Hosp Univ La Pitie Salpetriere, Unite Morphol Neuromusculaire, Ctr Reference Pathol Neuromusculaire Paris Est, Inst Myol, Paris, France UPMC Univ Paris 06, Univ Sorbonne, Grp Hosp Univ La Pitie Salpetriere, INSERM,UMRS974,CNRS,FRE3617,Ctr Res Myol, Paris, France Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainVilchez, Juan J.论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Politecn La Fe, Dept Neurol, Valencia, Spain Hosp Univ Politecn La Fe, IIS La Fe, Valencia, Spain Hosp Gen Univ Santa Lucia, Ctr Invest Biomed Red Enfermedades Raras CIBERER, Consulta Enfermedades Neuromusculares, Murcia, Spain Univ Valencia, Dept Med, Valencia, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainComas, David论文数: 0 引用数: 0 h-index: 0机构: Univ Pompeu Fabra, Dept Expt & Hlth Sci, Inst Evolutionary Biol, CSIC, Barcelona, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainLaing, Nigel G.论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Harry Perkins Inst Med Res, Nedlands, WA, Australia Univ Western Australia, Med Res Ctr, Nedlands, WA, Australia Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainLaporte, Jocelyn论文数: 0 引用数: 0 h-index: 0机构: IGBMC, Illkirch Graffenstaden, France CNRS, UMR7104, Illkirch Graffenstaden, France INSERM, U964, Illkirch Graffenstaden, France Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainKalaydjieva, Luba论文数: 0 引用数: 0 h-index: 0机构: Univ Western Australia, Harry Perkins Inst Med Res, Nedlands, WA, Australia Univ Western Australia, Med Res Ctr, Nedlands, WA, Australia Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, SpainParadas, Carmen论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, Spain Hosp Univ Virgen del Rocio, Inst Biomed Sevilla IBiS, Seville, Spain Hosp Univ Virgen del Rocio, Unidad Enfermedades Neuromusculares, Dept Neurol, Seville, Spain
- [27] A novel homozygous missense mutation in SLURP1 causes Mal de Meleda with an atypical phenotypeJOURNAL DER DEUTSCHEN DERMATOLOGISCHEN GESELLSCHAFT, 2011, 9 : 186 - 186Gruber, R.论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Dept Dermatol & Venereol, Innsbruck, Austria Innsbruck Med Univ, Dept Dermatol & Venereol, Innsbruck, AustriaHennies, H. C.论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Cologne Ctr Genom, Div Dermatogenet, Cologne, Germany Innsbruck Med Univ, Dept Dermatol & Venereol, Innsbruck, AustriaRomani, N.论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Dept Dermatol & Venereol, Innsbruck, Austria Innsbruck Med Univ, Dept Dermatol & Venereol, Innsbruck, AustriaSchmuth, M.论文数: 0 引用数: 0 h-index: 0机构: Innsbruck Med Univ, Dept Dermatol & Venereol, Innsbruck, Austria Univ Cologne, Cologne Ctr Genom, Div Dermatogenet, Cologne, Germany Innsbruck Med Univ, Dept Dermatol & Venereol, Innsbruck, Austria
- [28] A novel mutation in PLP1 causes severe hereditary spastic paraplegia type 2GENE, 2014, 533 (01) : 447 - 450Noetzli, Leila论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USA Univ Colorado Denver, Sch Med, Human Med Genet & Genom Program, Aurora, CO 80045 USA Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USASanz, Pablo G.论文数: 0 引用数: 0 h-index: 0机构: Hosp Espanol Buenos Aires, Dept Neurol, Buenos Aires, DF, Argentina Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USABrodsky, Gary L.论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USA Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USAHinckley, Jesse D.论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USA Univ Colorado Denver, Sch Med, Human Med Genet & Genom Program, Aurora, CO 80045 USA Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USAGiugni, Juan C.论文数: 0 引用数: 0 h-index: 0机构: Hosp Espanol Buenos Aires, Dept Neurol, Buenos Aires, DF, Argentina Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USAGiannaula, Rolando J.论文数: 0 引用数: 0 h-index: 0机构: Hosp Espanol Buenos Aires, Dept Neurol, Buenos Aires, DF, Argentina Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USAGonzalez-Alegre, Pedro论文数: 0 引用数: 0 h-index: 0机构: Univ Iowa, Dept Neurol, Iowa City, IA 52242 USA Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USADi Paola, Jorge论文数: 0 引用数: 0 h-index: 0机构: Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USA Univ Colorado Denver, Sch Med, Human Med Genet & Genom Program, Aurora, CO 80045 USA Univ Colorado Denver, Sch Med, Dept Pediat, Aurora, CO 80045 USA
- [29] A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier disease (vol 126, pg 920, 2003)BRAIN, 2003, 126 : 2115 - 2115Züchner, S论文数: 0 引用数: 0 h-index: 0Sperfeld, AD论文数: 0 引用数: 0 h-index: 0Senderek, J论文数: 0 引用数: 0 h-index: 0Sellhaus, B论文数: 0 引用数: 0 h-index: 0Hanemann, CO论文数: 0 引用数: 0 h-index: 0Schröder, JM论文数: 0 引用数: 0 h-index: 0
- [30] Severe XLP Phenotype Caused by a Novel Intronic Mutation in the SH2D1A GeneJournal of Clinical Immunology, 2015, 35 : 26 - 31B. Tóth论文数: 0 引用数: 0 h-index: 0机构: University of Debrecen,Department of Infectious Diseases and Pediatric Immunology, Faculty of MedicineB. Soltész论文数: 0 引用数: 0 h-index: 0机构: University of Debrecen,Department of Infectious Diseases and Pediatric Immunology, Faculty of MedicineE. Gyimesi论文数: 0 引用数: 0 h-index: 0机构: University of Debrecen,Department of Infectious Diseases and Pediatric Immunology, Faculty of MedicineG. Csorba论文数: 0 引用数: 0 h-index: 0机构: University of Debrecen,Department of Infectious Diseases and Pediatric Immunology, Faculty of MedicineÁ. Veres论文数: 0 引用数: 0 h-index: 0机构: University of Debrecen,Department of Infectious Diseases and Pediatric Immunology, Faculty of MedicineÁ. Lányi论文数: 0 引用数: 0 h-index: 0机构: University of Debrecen,Department of Infectious Diseases and Pediatric Immunology, Faculty of MedicineG. Kovács论文数: 0 引用数: 0 h-index: 0机构: University of Debrecen,Department of Infectious Diseases and Pediatric Immunology, Faculty of MedicineL. Maródi论文数: 0 引用数: 0 h-index: 0机构: University of Debrecen,Department of Infectious Diseases and Pediatric Immunology, Faculty of MedicineM. Erdős论文数: 0 引用数: 0 h-index: 0机构: University of Debrecen,Department of Infectious Diseases and Pediatric Immunology, Faculty of Medicine