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Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA

โœ Scribed by Litt, M


Book ID
125472070
Publisher
Oxford University Press
Year
1998
Tongue
English
Weight
99 KB
Volume
7
Category
Article
ISSN
0964-6906

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Hereditary cataract is a phenotypically and genetically heterogeneous lens disease that is responsible for a significant proportion of the visual impairment and blindness that occurs in children. In a five-generation Chinese family with autosomal dominant inherited congenital cataract, clinical exam