Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness
Nature Genetics1998Vol. 19(3), pp. 264–267
Citations Over TimeTop 10% of 1998 papers
Bech-Hansen Nt, Naylor Mj, Maybaum Ta, Pearce Wg, Ben F. Koop, Fishman Ga, M. B. Mets, Musarella Ma, Boycott Km
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