CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

✍ Scribed by Kohl, Susanne; Varsanyi, Balazs; Antunes, Gesine Abadin; Baumann, Britta; Hoyng, Carel B; Jägle, Herbert; Rosenberg, Thomas; Kellner, Ulrich; Lorenz, Birgit; Salati, Roberto

• Book ID: 110025674
• Publisher: Nature Publishing Group
• Year: 2004
• Tongue: English
• Weight: 109 KB
• Volume: 13
• Category: Article
• ISSN: 1018-4813
• DOI: 10.1038/sj.ejhg.5201269