Three novel mutations of the ornithine aminotransferase (OAT) gene in gyrate atrophy
- 31 October 1992
- Vol. 14 (2) , 553-554
- https://doi.org/10.1016/s0888-7543(05)80271-x
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
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- An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.Journal of Clinical Investigation, 1988
- Localization of the ornithine aminotransferase gene and related sequences on two human chromosomesHuman Genetics, 1987
- Investigation of Gyrate Atrophy Using a cDNA Clone for Human Ornithine AminotransferaseDNA, 1986