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G59S mutation in the GJB2 gene in a Chinese family with classic Vohwinkel syndrome.
Xie, Ming-Xing; Yang, Wei-Ping; Luo, Hao-Jie; Ismail, Ferina; Hao, Yang-Yang; Yang, Jian-Qiang.
Affiliation
  • Xie MX; Department of Dermatology, Changxing Hospital, Huzhou, China.
  • Yang WP; Department of Stomatology, The First Affiliated Hospital of Huzhou University, Huzhou, China.
  • Luo HJ; Department of Dermatology, The First Affiliated Hospital of Huzhou University, Huzhou, China.
  • Ismail F; Department of Dermatology, The Royal London Hospital, London, UK.
  • Hao YY; Department of Dermatology, The First Affiliated Hospital of Huzhou University, Huzhou, China.
  • Yang JQ; Department of Dermatology, The First Affiliated Hospital of Huzhou University, Huzhou, China.
J Dermatol ; 46(2): 154-157, 2019 Feb.
Article in En | MEDLINE | ID: mdl-30565282
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Hand Deformities, Congenital / Keratoderma, Palmoplantar / Connexins / Hearing Loss, Sensorineural Limits: Adult / Female / Humans Language: En Journal: J Dermatol Year: 2019 Type: Article Affiliation country: China
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Hand Deformities, Congenital / Keratoderma, Palmoplantar / Connexins / Hearing Loss, Sensorineural Limits: Adult / Female / Humans Language: En Journal: J Dermatol Year: 2019 Type: Article Affiliation country: China