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- [1] Molecular diagnosis and disease gene identification in neurological disorders using exome sequencingEUROPEAN JOURNAL OF NEUROLOGY, 2014, 21 : 94 - 94Haack, T. B.论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Inst Human Genet, D-80290 Munich, Germany Tech Univ Munich, Inst Human Genet, D-80290 Munich, GermanyFreisinger, P.论文数: 0 引用数: 0 h-index: 0机构: Community Hosp Reutlingen, Munich, Germany Tech Univ Munich, Inst Human Genet, D-80290 Munich, GermanyMayr, H.论文数: 0 引用数: 0 h-index: 0机构: Paracelsus Med Univ, Salzburg, Austria Tech Univ Munich, Inst Human Genet, D-80290 Munich, GermanySperl, W.论文数: 0 引用数: 0 h-index: 0机构: Paracelsus Med Univ, Salzburg, Austria Tech Univ Munich, Inst Human Genet, D-80290 Munich, GermanyKornblum, C.论文数: 0 引用数: 0 h-index: 0机构: Univ Bonn, Bonn, Germany Tech Univ Munich, Inst Human Genet, D-80290 Munich, GermanyKlopstock, T.论文数: 0 引用数: 0 h-index: 0机构: Univ Munich, Munich, Germany Tech Univ Munich, Inst Human Genet, D-80290 Munich, GermanyStrom, T. M.论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Inst Human Genet, D-80290 Munich, Germany Tech Univ Munich, Inst Human Genet, D-80290 Munich, GermanyMeitinger, T.论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Inst Human Genet, D-80290 Munich, Germany Tech Univ Munich, Inst Human Genet, D-80290 Munich, GermanyProkisch, H.论文数: 0 引用数: 0 h-index: 0机构: Tech Univ Munich, Inst Human Genet, D-80290 Munich, Germany Tech Univ Munich, Inst Human Genet, D-80290 Munich, Germany
- [2] Diagnosis and molecular basis of mitochondrial respiratory chain disorders: Exome sequencing for disease gene identificationBIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2014, 1840 (04): : 1355 - 1359Ohtake, A.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanMurayama, K.论文数: 0 引用数: 0 h-index: 0机构: Chiba Childrens Hosp, Dept Metab, Chiba 2660007, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanMori, M.论文数: 0 引用数: 0 h-index: 0机构: Jichi Med Univ, Dept Pediat, Shimotsuke, Tochigi 3290498, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanHarashima, H.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanYamazaki, T.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanTamaru, S.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Res Ctr Genom Med, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanYamashita, Y.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Res Ctr Genom Med, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanKishita, Y.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Res Ctr Genom Med, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanNakachi, Y.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Res Ctr Genom Med, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanKohda, M.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Res Ctr Genom Med, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanTokuzawa, Y.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Res Ctr Genom Med, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanMizuno, Y.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Res Ctr Genom Med, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanMoriyama, Y.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Res Ctr Genom Med, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanKato, H.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Res Ctr Genom Med, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, JapanOkazaki, Y.论文数: 0 引用数: 0 h-index: 0机构: Saitama Med Univ, Res Ctr Genom Med, Saitama 3500495, Japan Saitama Med Univ, Fac Med, Dept Pediat, Saitama 3500495, Japan
- [3] Exome sequencing for neurological disordersJOURNAL OF THE NEUROLOGICAL SCIENCES, 2017, 381 : 21 - 21Vance, J.论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, HIHG, Miami, FL 33136 USA Univ Miami, Miller Sch Med, HIHG, Miami, FL 33136 USATekin, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Miller Sch Med, HIHG, Miami, FL 33136 USA Univ Miami, Miller Sch Med, HIHG, Miami, FL 33136 USA
- [4] Disease gene identification by exome sequencingMEDIZINISCHE GENETIK, 2012, 24 (01) : 4 - +Neveling, K.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr Nijmegen, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr Nijmegen, Dept Human Genet, NL-6500 HB Nijmegen, NetherlandsHoischen, A.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr Nijmegen, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr Nijmegen, Dept Human Genet, NL-6500 HB Nijmegen, Netherlands
- [5] Disease gene identification strategies for exome sequencingEUROPEAN JOURNAL OF HUMAN GENETICS, 2012, 20 (05) : 490 - 497Gilissen, Christian论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Inst Genet & Metab Disorders, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, NetherlandsHoischen, Alexander论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Inst Genet & Metab Disorders, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, NetherlandsBrunner, Han G.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Inst Genet & Metab Disorders, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, NetherlandsVeltman, Joris A.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Inst Genet & Metab Disorders, NL-6500 HB Nijmegen, Netherlands Radboud Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands
- [6] Disease gene identification strategies for exome sequencingEuropean Journal of Human Genetics, 2012, 20 : 490 - 497Christian Gilissen论文数: 0 引用数: 0 h-index: 0机构: Nijmegen Centre for Molecular Life Sciences and Institute for Genetic and Metabolic Disorders,Department of Human GeneticsAlexander Hoischen论文数: 0 引用数: 0 h-index: 0机构: Nijmegen Centre for Molecular Life Sciences and Institute for Genetic and Metabolic Disorders,Department of Human GeneticsHan G Brunner论文数: 0 引用数: 0 h-index: 0机构: Nijmegen Centre for Molecular Life Sciences and Institute for Genetic and Metabolic Disorders,Department of Human GeneticsJoris A Veltman论文数: 0 引用数: 0 h-index: 0机构: Nijmegen Centre for Molecular Life Sciences and Institute for Genetic and Metabolic Disorders,Department of Human Genetics
- [7] Molecular diagnosis of McArdle disease using whole-exome sequencingEXPERIMENTAL AND THERAPEUTIC MEDICINE, 2021, 22 (03)Kang, Ju-Hyung论文数: 0 引用数: 0 h-index: 0机构: Eulji Univ, Sch Med, Dept Pediat, Daejeon 34824, South Korea Eulji Univ, Sch Med, Dept Pediat, Daejeon 34824, South KoreaPark, Jun-Hyung论文数: 0 引用数: 0 h-index: 0机构: Eulji Univ, Sch Med, Dept Biochem & Mol Biol, 77 Gyeryong Ro,771 Gil, Daejeon 34824, South Korea Eulji Univ, Sch Med, Dept Pediat, Daejeon 34824, South KoreaPark, Jin-Soon论文数: 0 引用数: 0 h-index: 0机构: Eulji Univ, Sch Med, Dept Biochem & Mol Biol, 77 Gyeryong Ro,771 Gil, Daejeon 34824, South Korea Eulji Univ, Sch Med, Dept Pediat, Daejeon 34824, South KoreaLee, Seong-Kyu论文数: 0 引用数: 0 h-index: 0机构: Eulji Univ, Sch Med, Dept Biochem & Mol Biol, 77 Gyeryong Ro,771 Gil, Daejeon 34824, South Korea Eulji Univ, Sch Med, Dept Pediat, Daejeon 34824, South KoreaLee, Sunghoon论文数: 0 引用数: 0 h-index: 0机构: Eone Diagn Genome Ctr, Dept Res & Dev, Incheon 22014, South Korea Eulji Univ, Sch Med, Dept Pediat, Daejeon 34824, South KoreaBaik, Haing-Woon论文数: 0 引用数: 0 h-index: 0机构: Eulji Univ, Sch Med, Dept Biochem & Mol Biol, 77 Gyeryong Ro,771 Gil, Daejeon 34824, South Korea Eulji Univ, Sch Med, Dept Pediat, Daejeon 34824, South Korea
- [8] Use of Targeted Exome Sequencing for Molecular Diagnosis of Skeletal DisordersPLOS ONE, 2015, 10 (09):Polla, Daniel L.论文数: 0 引用数: 0 h-index: 0机构: Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, BrazilCardoso, Maria T. O.论文数: 0 引用数: 0 h-index: 0机构: Nucleo Genet Secretaria Saude Dist Fed, Brasilia, DF, Brazil Univ Catolica Brasilia, Curso Med, Taguatinga, DF, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, BrazilSilva, Mayara C. B.论文数: 0 引用数: 0 h-index: 0机构: Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, BrazilCardoso, Isabela C. C.论文数: 0 引用数: 0 h-index: 0机构: Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, BrazilMedina, Cristina T. N.论文数: 0 引用数: 0 h-index: 0机构: Nucleo Genet Secretaria Saude Dist Fed, Brasilia, DF, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, BrazilAraujo, Rosenelle论文数: 0 引用数: 0 h-index: 0机构: Nucleo Genet Secretaria Saude Dist Fed, Brasilia, DF, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, BrazilFernandes, Camila C.论文数: 0 引用数: 0 h-index: 0机构: Univ Estadual Paulista, Fac Ciencias Agr & Vet, Dept Tecnol, Lab Multiusuario Centralizado Sequenciamento DNA, Jaboticabal, SP, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, BrazilReis, Alessandra M. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, Brazilde Andrade, Rosangela V.论文数: 0 引用数: 0 h-index: 0机构: Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, BrazilPereira, Rinaldo W.论文数: 0 引用数: 0 h-index: 0机构: Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, BrazilPogue, Robert论文数: 0 引用数: 0 h-index: 0机构: Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, Brazil Univ Catolica Brasilia, Programa Posgrad Ciencias Genom & Biotecnol, Brasilia, DF, Brazil
- [9] Genetic diagnosis of neuroacanthocytosis disorders using exome sequencingMOVEMENT DISORDERS, 2012, 27 (04) : 539 - 543Walker, Ruth H.论文数: 0 引用数: 0 h-index: 0机构: James J Peters Vet Affairs Med Ctr, Dept Neurol, Bronx, NY 10468 USA Mt Sinai Sch Med, Dept Neurol, New York, NY USA James J Peters Vet Affairs Med Ctr, Dept Neurol, Bronx, NY 10468 USASchulz, Vincent P.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06510 USA James J Peters Vet Affairs Med Ctr, Dept Neurol, Bronx, NY 10468 USATikhonova, Irina R.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA Yale Univ, Yale Ctr Genome Anal, Orange, CT USA James J Peters Vet Affairs Med Ctr, Dept Neurol, Bronx, NY 10468 USAMahajan, Milind C.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA Yale Univ, Yale Ctr Genome Anal, Orange, CT USA James J Peters Vet Affairs Med Ctr, Dept Neurol, Bronx, NY 10468 USAMane, Shrikant论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA Yale Univ, Yale Ctr Genome Anal, Orange, CT USA James J Peters Vet Affairs Med Ctr, Dept Neurol, Bronx, NY 10468 USAMuniz, Maritza Arroyo论文数: 0 引用数: 0 h-index: 0机构: Univ Puerto Rico, Dept Med, Neurol Sect, San Juan, PR 00936 USA James J Peters Vet Affairs Med Ctr, Dept Neurol, Bronx, NY 10468 USAGallagher, Patrick G.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06510 USA Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA James J Peters Vet Affairs Med Ctr, Dept Neurol, Bronx, NY 10468 USA
- [10] Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a modelBRAIN, 2013, 136 : 3106 - 3118Nemeth, Andrea H.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England Oxford Univ Hosp NHS Trust, Churchill Hosp, Dept Clin Genet, Oxford OX3 7LJ, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandKwasniewska, Alexandra C.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandLise, Stefano论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandSchnekenberg, Ricardo Parolin论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Posit, Sch Med, Curitiba, Parana, Brazil Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandBecker, Esther B. E.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, MRC Funct Genom Unit, Dept Physiol Anat & Genet, Oxford OX1 3QX, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandBera, Katarzyna D.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, MRC Funct Genom Unit, Dept Physiol Anat & Genet, Oxford OX1 3QX, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandShanks, Morag E.论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandGregory, Lorna论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandBuck, David论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandCader, M. Zameel论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandTalbot, Kevin论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandDe Silva, Rajith论文数: 0 引用数: 0 h-index: 0机构: Queens Hosp, Essex Ctr Neurol Sci, Dept Neurol, Romford, Essex, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandFletcher, Nicholas论文数: 0 引用数: 0 h-index: 0机构: Walton Ctr NHS Fdn Trust, Liverpool L9 7LJ, Merseyside, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandHastings, Rob论文数: 0 引用数: 0 h-index: 0机构: St Michaels Hosp, Dept Clin Genet, Bristol BS2 8EG, Avon, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandJayawant, Sandeep论文数: 0 引用数: 0 h-index: 0机构: Oxford Univ Hosp NHS Trust, Dept Paediat, Oxford OX3 7LJ, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandMorrison, Patrick J.论文数: 0 引用数: 0 h-index: 0机构: Queens Univ Belfast, Sch Med Dent & Biomed Sci, Belfast BT9 7BL, Antrim, North Ireland Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandWorth, Paul论文数: 0 引用数: 0 h-index: 0机构: Norfolk & Norwich Univ Hosp, Dept Neurol, Norwich, Norfolk, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandTaylor, Malcolm论文数: 0 引用数: 0 h-index: 0机构: Univ Birmingham, Sch Canc Sci, Birmingham B15 2TT, W Midlands, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandTolmie, John论文数: 0 引用数: 0 h-index: 0机构: So Gen Hosp, Dept Clin Genet, Glasgow G51 4TF, Lanark, Scotland Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandO'Regan, Mary论文数: 0 引用数: 0 h-index: 0机构: Royal Hosp Sick Children, Fraser Allander Neurosci Unit, Glasgow G3 8SJ, Lanark, Scotland Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandConsortium, Uk Ataxia论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandValentine, Ruth论文数: 0 引用数: 0 h-index: 0机构: Thames Valley Dementia & Neurodegenerat Dis Netwo, Oxford, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandPackham, Emily论文数: 0 引用数: 0 h-index: 0机构: Oxford Univ Hosp NHS Trust, Oxford Reg Mol Genet Labs, Oxford OX3 7LJ, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England论文数: 引用数: h-index:机构:Seller, Anneke论文数: 0 引用数: 0 h-index: 0机构: Oxford Univ Hosp NHS Trust, Oxford Reg Mol Genet Labs, Oxford OX3 7LJ, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, EnglandRagoussis, Jiannis论文数: 0 引用数: 0 h-index: 0机构: Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England Univ Oxford, Nuffield Dept Clin Neurosci, Oxford OX3 9DU, England