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Intraretinal distribution of the ornithine aminotransferase (OAT) molecule and its activity

โœ Scribed by Kato, Takahiko; Hashida, Seiichi; Ishikawap, Eiji

Book ID
122556674
Publisher
Elsevier Science
Year
1991
Weight
91 KB
Volume
14
Category
Article
ISSN
0921-8696

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A 15-bp deletion in exon 5 of the ornith
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โœ James K. Park; James J. O'Donnell; Vivian E. Shih; James F. Gusella; Vijaya Rame ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 511 KB

Communicated by David W. Yandell Gyrate atrophy of the choroid and retina (GA) is an autosomal recessive disorder in which a deficiency of the mitochondrial matrix enzyme ornithine aminotransferase (OAT) leads to progressive blindness. Previously, we and others have reported a number of missense mut