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Nat Genet. 1998 Jul;19(3):260-3.

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.

Author information

  • 1Abteilung Medizinische Genetik der Ludwig-Maximilians-Universität, München, Germany.

Abstract

The locus for the incomplete form of X-linked congenital stationary night blindness (CSNB2) maps to a 1.1-Mb region in Xp11.23 between markers DXS722 and DXS255. We identified a retina-specific calcium channel alpha1-subunit gene (CACNA1F) in this region, consisting of 48 exons encoding 1966 amino acids and showing high homology to L-type calcium channel alpha1-subunits. Mutation analysis in 13 families with CSNB2 revealed nine different mutations in 10 families, including three nonsense and one frameshift mutation. These data indicate that aberrations in a voltage-gated calcium channel, presumably causing a decrease in neurotransmitter release from photoreceptor presynaptic terminals, are a frequent cause of CSNB2.

PMID:
9662399
[PubMed - indexed for MEDLINE]
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