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[A generalized deficiency in the mitochondrial enzyme, ornithine aminotransferase (OAT: EC 2.6.1.13), is the hallmark of gyrate atrophy (GA), a hereditary degenerative disease of the choroid and retina of the eye that leads to blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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