News doi:10.1038/947 Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness N. Torben Bech-Hansen Margaret J. Naylor Tracy A. Maybaum William G. Pearce Ben Koop Gerald A. Fishman Marilyn Mets Maria A. Musarella & Kym M. Boycott This article appears in: Nature Genetics 19, 264 - 267 (01 July 1998)
Nature Genetics 19, 264 - 267 (01 July 1998)
