A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants

Overview of attention for article published in Human Genetics, February 2001

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Cav1.4

Cited by user Tisfoon on 30 Dec 2018

X-linked congenital stationary night blindness

Cited by user DOI bot on 07 Jun 2008

X-linked congenital stationary night blindness (CSNB) is a rare X-linked non-progressive retinal disorder.

Cav1.4

Cited by user ProteinBoxBot on 18 Dec 2007

Cav1.4 also known as the calcium channel, voltage-dependent, L type, alpha 1F subunit (CACNA1F), is a human gene.