Clinical manifestations of a unique X-linked retinal...

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

Carolyn I Hope, Dianne M Sharp, Ariana Hemara-Wahanui, Jennifer I Sissingh, Patricia Lundon, Ed A Mitchell, Marion A Maw, Gillian M Clover
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Volume:
33
Year:
2005
Language:
english
Pages:
8
DOI:
10.1111/j.1442-9071.2005.00987.x
File:
PDF, 1.03 MB
english, 2005
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