The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 gene

✍ Scribed by Patrizia Amati-Bonneau; Sylvie Odent; Christelle Derrien; Laurent Pasquier; Yves Malthiéry; Pascal Reynier; Dominique Bonneau

• Book ID: 117019267
• Publisher: Elsevier Science
• Year: 2003
• Tongue: English
• Weight: 68 KB
• Volume: 136
• Category: Article
• ISSN: 0002-9394
• DOI: 10.1016/s0002-9394(03)00665-2