Functional analysis of congenital stationary night blindness type-2 CACNA1F mutations F742C, G1007R, and R1049W

✍ Scribed by J.B. Peloquin; R. Rehak; C.J. Doering; J.E. McRory

• Book ID: 116788307
• Publisher: Elsevier Science
• Year: 2007
• Tongue: English
• Weight: 605 KB
• Volume: 150
• Category: Article
• ISSN: 0306-4522
• DOI: 10.1016/j.neuroscience.2007.09.021