Clinical and Biochemical Heterogeneity in Gyrate Atrophy
- 1 February 1980
- journal article
- case report
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 89 (2) , 219-222
- https://doi.org/10.1016/0002-9394(80)90114-2
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- VITAMIN B6 IN MANAGEMENT OF GYRATE ATROPHY OF CHOROID AND RETINAThe Lancet, 1978
- Ocular and Biochemical Abnormalities in Gyrate Atrophy of the Choroid and RetinaOphthalmology, 1978
- Hyperornithinemia and Gyrate Atrophy of the Choroid and RetinaOphthalmology, 1978
- Gyrate Atrophy of the Retina: Inborn Error of L-Ornithin:2-Oxoacid AminotransferaseScience, 1978
- A Specific Enzyme Defect in Gyrate AtrophyAmerican Journal of Ophthalmology, 1978
- Gyrate Atrophy of Choroid and Retina: Deficient Activity of Ornithine Ketoacid Aminotransferase in Cultured Skin FibroblastsNew England Journal of Medicine, 1977
- Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes.Proceedings of the National Academy of Sciences, 1977
- l-Ornithine-ketoacid-transaminase deficiency in cultured fibroblasts of a patient with hyperornithinaemia and gyrate atrophy of the choroid and retinaClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- Genetic HeterogeneityNew England Journal of Medicine, 1968