A summary of 20CACNA1Fmutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

✍ Scribed by Kym Boycott; Tracy Maybaum; Margaret Naylor; Richard Weleber; Johane Robitaille; Yozo Miyake; Arthur Bergen; Mary Pierpont; William Pearce; N. Bech-Hansen

• Publisher: Springer
• Year: 2001
• Tongue: English
• Weight: 160 KB
• Volume: 108
• Category: Article
• ISSN: 0340-6717
• DOI: 10.1007/s004390100461