نتائج البحث

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.

• Authors : Hope CI; Department of Ophthalmology, University of Auckland, Auckland, New Zealand. ; Sharp DM

Subjects: Mutation*; Calcium Channels, L-Type/Calcium Channels, L-Type/Calcium Channels, L-Type/*genetics ; Genetic Diseases, X-Linked/Genetic Diseases, X-Linked/Genetic Diseases, X-Linked/*diagnosis

• Source: Clinical & experimental ophthalmology [Clin Exp Ophthalmol] 2005 Apr; Vol. 33 (2), pp. 129-36.Publisher: Wiley-Blackwell Pub. Asia Country of Publication: Australia NLM ID: 100896531 Publication Model: Print Cited Medium: Print ISSN:

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