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    Results: 3

    1.

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

    Hemara-Wahanui A, Berjukow S, Hope CI, Dearden PK, Wu SB, Wilson-Wheeler J, Sharp DM, Lundon-Treweek P, Clover GM, Hoda JC, Striessnig J, Marksteiner R, Hering S, Maw MA.

    Proc Natl Acad Sci U S A. 2005 May 24;102(21):7553-8. Epub 2005 May 16.PMID: 15897456 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2.

    Hope CI, Sharp DM, Hemara-Wahanui A, Sissingh JI, Lundon P, Mitchell EA, Maw MA, Clover GM.

    Clin Experiment Ophthalmol. 2005 Apr;33(2):129-36.PMID: 15807819 [PubMed - indexed for MEDLINE]Related articles

    3.

    Usher syndrome in the city of Birmingham--prevalence and clinical classification.

    Hope CI, Bundey S, Proops D, Fielder AR.

    Br J Ophthalmol. 1997 Jan;81(1):46-53.PMID: 9135408 [PubMed - indexed for MEDLINE]Related articlesFree article

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