Phenotype of three consanguineous Tunisian families with early-onset retinal degeneration caused by an R91W homozygous mutation in the RPE65 gene

✍ Scribed by Leila El Matri; Aude Ambresin; Daniel F. Schorderet; Aki Kawasaki; Mathias W. Seeliger; Andreas Wenzel; Yvan Arsenijevic; François‐Xavier Borruat; Francis L. Munier

• Publisher: Springer-Verlag
• Year: 2006
• Tongue: English
• Weight: 284 KB
• Volume: 244
• Category: Article
• ISSN: 0065-6100
• DOI: 10.1007/s00417-005-0096-2