Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes

Author:

Ramesh Vijaya,Eddy Roger,Bruns Gail A.,Shih Vivian E.,Shows Thomas B.,Gusella James F.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. Askanas V, Valle D, Kaiser-Kupfer MI, Takki K, Engel WK, Blumenkopf B (1980) Cultured muscle fibers of gyrate atrophy patients: tubules, ornithine toxicity and OAT deficiency. Neurology (NY) 30:368

2. Bhattacharya SS, Wright AF, Clayton JF, Price WH, Phillips CI, McKeown CME,Jay M, Bird AC, Pearson PL, Southern EM, Evans HJ (1984) Close linkage between X-linked retinitis pigmentosum and a restriction fragment polymorphism identified by recombinant DNA probe L1 28. Nature 309:253?255

3. Bruns GAP, Gusella JF, Keys C, Leary AC, Housman D, Gerald PS (1982) Isolation of X-chromosome DNA sequences. Adv Exp Med Biol 154:60?72

4. Feinberg AP, Vogelstein B (1983) A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 137:266?267

5. Gal A, Bleeker-Wagemakers L, Wienker TF, Warburg M, Ropers HH (1985) Localization of the gene for Norrie disease by linkage to the DXS7 locus. Cytogenet Cell Genet 40:633

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