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Year | Number of Results |
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1997 | 1 |
2005 | 2 |
2023 | 0 |
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A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.
Proc Natl Acad Sci U S A. 2005 May 24;102(21):7553-8. doi: 10.1073/pnas.0501907102. Epub 2005 May 16.
Proc Natl Acad Sci U S A. 2005.
PMID: 15897456
Free PMC article.
Usher syndrome in the city of Birmingham--prevalence and clinical classification.
Hope CI, Bundey S, Proops D, Fielder AR.
Hope CI, et al.
Br J Ophthalmol. 1997 Jan;81(1):46-53. doi: 10.1136/bjo.81.1.46.
Br J Ophthalmol. 1997.
PMID: 9135408
Free PMC article.
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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.
Hope CI, et al.
Clin Exp Ophthalmol. 2005 Apr;33(2):129-36. doi: 10.1111/j.1442-9071.2005.00987.x.
Clin Exp Ophthalmol. 2005.
PMID: 15807819
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