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Gene mutations in retinitis pigmentosa and their clinical implications

โœ Scribed by D.Y. Wang; W.M. Chan; P.O.S. Tam; L. Baum; D.S.C. Lam; K.K.L. Chong; B.J. Fan; C.P. Pang


Book ID
116349985
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
160 KB
Volume
351
Category
Article
ISSN
0009-8981

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Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form (adRP), which comprises about 25% of total cases, app