A Specific Enzyme Defect in Gyrate Atrophy
Author:
Publisher
Elsevier BV
Subject
Ophthalmology
Reference13 articles.
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2. Genetic aspects in gyrate atrophy of the choroid and retina with hyperornithinemia;Takki;Br. J. Ophthalmol.,1974
3. Plasma amino-acids in hereditary retinal disease;Berson;Br. J. Ophthalmol.,1976
4. Ornithine (ORN) metabolism and liver pathology in hyperornithinemia and gyrate atrophy of the choroid and retina (HOGA);Arshiroff;Clin. Res.,1977
5. Increased sensitivity of lymphocyte δ1-pyrroline-5-carboxylate reductase to inhibition by proline with transformation;Valle;Nature,1975
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3. OAT mutations and clinical features in two Japanese brothers with gyrate atrophy of the choroid and retina;Documenta Ophthalmologica;2014-01-16
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