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[A novel mutation of the type 1 optic atrophy(OPA1) gene in a Japanese family with OPA1].
Shimizu, Satoko; Mori, Naoki; Kishi, Mari; Sugata, Hirohisa; Tsuda, Akiko; Kubota, Nobue.
Affiliation
  • Shimizu S; Department of Ophthalmology, Teikyo University School of Medicine, 2-11-1 Kaga, Itabashi-ku, Tokyo 173-8605, Japan.
Nippon Ganka Gakkai Zasshi ; 106(7): 398-403, 2002 Jul.
Article in Ja | MEDLINE | ID: mdl-12187822
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Collection: 01-internacional Database: MEDLINE Main subject: Optic Atrophy / GTP Phosphohydrolases / Mutation Type of study: Diagnostic_studies Limits: Child / Humans / Male Language: Ja Journal: Nippon Ganka Gakkai Zasshi Year: 2002 Document type: Article Affiliation country: Japan Country of publication: Japan
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Optic Atrophy / GTP Phosphohydrolases / Mutation Type of study: Diagnostic_studies Limits: Child / Humans / Male Language: Ja Journal: Nippon Ganka Gakkai Zasshi Year: 2002 Document type: Article Affiliation country: Japan Country of publication: Japan