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Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family.
Wang, Longhao; Zhao, Lin; Peng, Hu; Xu, Jun; Lin, Yun; Yang, Tao; Wu, Hao.
Afiliação
  • Wang L; Department of Otorhinolaryngology-Head and Neck Surgery, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.
  • Zhao L; Ear Institute, Shanghai Jiao Tong University School of Medicine, Shanghai 200125, China.
  • Peng H; Shanghai Key Laboratory of Translational Medicine on Ear and Nose Diseases, Shanghai 200125, China.
  • Xu J; Department of Health Management Center, Shanghai Eastern Hepatobiliary Surgery Hospital, Shanghai 200438, China.
  • Lin Y; Ear Institute, Shanghai Jiao Tong University School of Medicine, Shanghai 200125, China.
  • Yang T; Shanghai Key Laboratory of Translational Medicine on Ear and Nose Diseases, Shanghai 200125, China.
  • Wu H; Department of Otorhinolaryngology-Head and Neck Surgery, Changzheng Hospital, Second Military Medical University, Shanghai 200003, China.
Neural Plast ; 2020: 6350479, 2020.
Article em En | MEDLINE | ID: mdl-32617096
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Miosinas / Implante Coclear / Surdez / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Miosinas / Implante Coclear / Surdez / Mutação Tipo de estudo: Prognostic_studies Limite: Adolescent / Humans / Male País como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article