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Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome.
Yotsumoto, S; Hashiguchi, T; Chen, X; Ohtake, N; Tomitaka, A; Akamatsu, H; Matsunaga, K; Shiraishi, S; Miura, H; Adachi, J; Kanzaki, T.
Affiliation
  • Yotsumoto S; Department of Dermatology, Kagoshima University Faculty of Medicine, 8-35-1 Sakuragaoka, Kagoshima 890-8520, Japan. syotsumo@m2.kufm.kagoshima-u.ac.jp
Br J Dermatol ; 148(4): 649-53, 2003 Apr.
Article in En | MEDLINE | ID: mdl-12752120
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Collection: 01-internacional Database: MEDLINE Main subject: Connexins / Mutation, Missense / Ichthyosis / Keratitis Type of study: Prognostic_studies Limits: Adult / Child, preschool / Female / Humans / Male Language: En Journal: Br J Dermatol Year: 2003 Document type: Article Affiliation country: Japón Country of publication: Reino Unido
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Connexins / Mutation, Missense / Ichthyosis / Keratitis Type of study: Prognostic_studies Limits: Adult / Child, preschool / Female / Humans / Male Language: En Journal: Br J Dermatol Year: 2003 Document type: Article Affiliation country: Japón Country of publication: Reino Unido