| scholarly article | Q13442814 |
| P50 | author | James F. Gusella | Q1602688 |
| P2093 | author name string | T B Shows | |
| V Ramesh | |||
| V E Shih | |||
| P Crawford | |||
| P T Harvey | |||
| L A Benoit | |||
| P2860 | cites work | "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum | Q27860612 |
| Precise localization of human beta-globin gene complex on chromosome 11 | Q34038317 | ||
| A polymorphic DNA marker genetically linked to Huntington's disease | Q34255139 | ||
| Gyrate atrophy of the choroid and retina: deficiency of ornithine aminotransferase in transformed lymphocytes | Q35062416 | ||
| Ornithine ketoacid transaminase deficiency in gyrate atrophy of the choroid and retina | Q35202683 | ||
| Selective isolation of cosmid clones by homologous recombination in Escherichia coli | Q36264772 | ||
| Gyrate atrophy of the choroid and retina with hyperornithinemia: characterization of mutant liver L-ornithine:2-oxoacid aminotransferase kinetics | Q37000425 | ||
| Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines | Q45795446 | ||
| Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferase | Q48355109 | ||
| Deficient L-ornithine: 2-oxoacid aminotransferase activity in cultured fibroblasts from a patient with gyrate atrophy of the retina | Q67039097 | ||
| Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes | Q69902891 | ||
| L-Ornithine ketoacid-transaminase assay in hair roots of homozygotes and heterozygotes for gyrate atrophy | Q70823227 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 365-372 | |
| P577 | publication date | 1988-02-01 | |
| P1433 | published in | American Journal of Human Genetics | Q4744249 |
| P1476 | title | The ornithine aminotransferase (OAT) locus: analysis of RFLPs in gyrate atrophy | |
| P478 | volume | 42 |
| Q33889515 | Allelic loss of chromosomes 16q and 10q in human prostate cancer |
| Q90078747 | Cystoid macular edema secondary to gyrate atrophy in a child treated with sub-tenon injection of triamcinolone acetonide |
| Q35248235 | Gyrate atrophy of the choroid and retina: assignment of the ornithine aminotransferase structural gene to human chromosome 10 and mouse chromosome 7. |
| Q45405417 | 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 |
| Q30502692 | Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase |
| Q44040255 | Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3 |
| Q33576824 | Molecular basis of ornithine aminotransferase deficiency in B-6-responsive and -nonresponsive forms of gyrate atrophy |
| Q28305909 | OAT mutations and clinical features in two Japanese brothers with gyrate atrophy of the choroid and retina |
| Q40792353 | Ophthalmology in the post-genomic era |
| Q33596248 | Recent advances in the gene map of inherited eye disorders: primary hereditary diseases of the retina, choroid, and vitreous |
| Q35198033 | Splicing defect at the ornithine aminotransferase (OAT) locus in gyrate atrophy |
| Q36248188 | The ornithine aminotransferase gene in gyrate atrophy of the retina: analysis of expression and gross structure of this gene in cultured fibroblasts |
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