We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleLoss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.AuthorsBech-Hansen NT; Naylor MJ; Maybaum TA; Pearce WG; Koop B; Fishman GA; Mets M; Musarella MA; Boycott KMPublicationNature genetics, 1998, Vol 19, Issue 3, p264ISSN1061-4036Publication typearticleDOI10.1038/947