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Items: 4

1.

Mutations in the CACNA1F and NYX genes in British CSNBX families.

Zito I, Allen LE, Patel RJ, Meindl A, Bradshaw K, Yates JR, Bird AC, Erskine L, Cheetham ME, Webster AR, Poopalasundaram S, Moore AT, Trump D, Hardcastle AJ.

Hum Mutat. 2003 Feb;21(2):169.

PMID:
12552565
2.

[Molecular genetic study of congenital stationary night blindness].

Nakamura M, Miyake Y.

Nippon Ganka Gakkai Zasshi. 2004 Nov;108(11):665-73. Review. Japanese.

PMID:
15584351
3.

[Establishment of the concept of new clinical entities--complete and incomplete form of congenital stationary night blindness].

Miyake Y.

Nippon Ganka Gakkai Zasshi. 2002 Dec;106(12):737-55; discussion 756. Review. Japanese.

PMID:
12610835
4.

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

Doering CJ, Peloquin JB, McRory JE.

Channels (Austin). 2007 Jan-Feb;1(1):3-10. Epub 2007 Jan 1. Review.

PMID:
19151588

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