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A 15-bp deletion in exon 5 of the ornithine aminotransferase (OAT) locus associated with gyrate atrophy.
Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3.
Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiency.
Splicing defect at the ornithine aminotransferase (OAT) locus in gyrate atrophy.
Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferase.
Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes.
The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy.
The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10.
Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophy.