The ornithine aminotransferase (OAT) locus is linked and distal to D10S20 on the long arm of chromosome 10
Author:
Publisher
S. Karger AG
Subject
Genetics (clinical),Genetics,Molecular Biology
Cited by 15 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Degenerative Night-Blinding Disorders and Cone and Cone–Rod Dystrophies;Handbook of Clinical Electrophysiology of Vision;2019
2. OAT mutations and clinical features in two Japanese brothers with gyrate atrophy of the choroid and retina;Documenta Ophthalmologica;2014-01-16
3. Gyrate atrophy: clinical and genetic findings in a female without arginine-restricted diet during her first 39 years of life and report of a new OAT gene mutation;Documenta Ophthalmologica;2012-06-07
4. Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous.;Journal of Medical Genetics;1994-12-01
5. Comparative map for mice and humans;Mammalian Genome;1992-09
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