Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness
Bech-Hansen Nt(University of Calgary), Naylor Mj(University of Calgary), Maybaum Ta(University of Calgary), Pearce Wg(University of Alberta), Ben F. Koop(University of Victoria), Fishman Ga(University of Illinois Urbana-Champaign), M. B. Mets(Lurie Children's Hospital), Maria A. Musarella(University of Toronto), Boycott Km(University of Calgary)
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