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Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

✍ Scribed by Bech-Hansen, N. Torben; Naylor, Margaret J.; Maybaum, Tracy A.; Pearce, William G.; Koop, Ben; Fishman, Gerald A.; Mets, Marilyn; Musarella, Maria A.; Boycott, Kym M.

Book ID: 109832158
Publisher: Nature Publishing Group
Year: 1998
Tongue: English
Weight: 176 KB
Volume: 19
Category: Article
ISSN: 1061-4036
DOI: 10.1038/947

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