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An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
Nat Genet. 1998 Jul;19(3):260-3. doi: 10.1038/940.
Nat Genet. 1998.
PMID: 9662399
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
Bech-Hansen NT, Naylor MJ, Maybaum TA, Pearce WG, Koop B, Fishman GA, Mets M, Musarella MA, Boycott KM.
Bech-Hansen NT, et al.
Nat Genet. 1998 Jul;19(3):264-7. doi: 10.1038/947.
Nat Genet. 1998.
PMID: 9662400
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