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A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss.
Wang, Mingming; Zhou, Yicui; Zhang, Fengguo; Fan, Zhaomin; Bai, Xiaohui; Wang, Haibo.
Affiliation
  • Wang M; Department of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial ENT Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
  • Zhou Y; Department of Otorhinolaryngology Head and Neck Surgery, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
  • Zhang F; Shandong Institute of Otolaryngology, Shandong Provincial ENT Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
  • Fan Z; Department of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial ENT Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.
  • Bai X; Shandong Institute of Otolaryngology, Shandong Provincial ENT Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China. baixiaohui@sdu.edu.cn.
  • Wang H; Department of Clinical Laboratory, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China. baixiaohui@sdu.edu.cn.
BMC Med Genet ; 21(1): 154, 2020 07 25.
Article in En | MEDLINE | ID: mdl-32711451
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Full text: 1 Database: MEDLINE Main subject: Myosin Heavy Chains / Myosin Type II / Asian People / Genes, Dominant / Hearing Loss, Sensorineural / Mutation Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Year: 2020 Type: Article
Fulltext
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PubMed Links
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Full text: 1 Database: MEDLINE Main subject: Myosin Heavy Chains / Myosin Type II / Asian People / Genes, Dominant / Hearing Loss, Sensorineural / Mutation Type of study: Prognostic_studies Limits: Female / Humans / Male Language: En Year: 2020 Type: Article