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Article

The Ca(v)1.4 calcium channel: more than meets the eye.

Channels (Austin, Tex.) - 1 Jan 2000

Doering Clinton J, Peloquin Jean B, McRory John E

Abstract excerpt

Ca(v)1.4 channels are the latest calcium channels to be described in the literature. Originally identified in 1997 from the human genome project, several reports have since been published describing mutations in the CACNA1F gene encoding Ca(v)1.4 channels, and implicated these mutations in human disorders such as X-linked cone rod dystrophy (CORDX3) and incomplete X-linked congenital stationary night blindness...

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Identifiers

PMID: 19151588

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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The Ca(v)1.4 calcium channel: more than meets the eye.PMID 19151588Read ↗

A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.Semantic proximity Read ↗

The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution.Semantic proximity Read ↗

Cav1.4 dysfunction and congenital stationary night blindness type 2.Semantic proximity Read ↗

Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.Semantic proximity Read ↗

Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.Semantic proximity Read ↗

Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2.Semantic proximity Read ↗

Congenital stationary night blindness type 2 mutations S229P, G369D, L1068P, and W1440X alter channel gating or functional expression of Ca(v)1.4 L-type Ca2+ channels.Semantic proximity Read ↗

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.Semantic proximity Read ↗

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

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Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina.Semantic proximity Read ↗

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