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Activation-induced changes in alternate splice acceptor site usage

โœ Scribed by T. Prescott Atkinson; Yuling Dai

Book ID
116294921
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
152 KB
Volume
358
Category
Article
ISSN
0006-291X

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Gyrate atrophy (GA) is an autosomal recessive eye disease involving a progressive loss of vision due to chorioretinal degeneration in which the mitochondrial matrix enzyme ornithine aminotransferase (OAT) is defective. Two sisters with GA are described in this study in whom an A-to-G substitution at