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49. The sparse fur mouse as a model for gene therapy in ornithine carbamoyltransferase deficiency. Batshaw ML; Yudkoff M; McLaughlin BA; Gorry E; Anegawa NJ; Smith IA; Hyman SL; Robinson MB Gene Ther; 1995 Dec; 2(10):743-9. PubMed ID: 8750014 [TBL] [Abstract][Full Text] [Related]
50. Seven new mutations in the human ornithine transcarbamylase gene. Tuchman M; Plante RJ; McCann MT; Qureshi AA Hum Mutat; 1994; 4(1):57-60. PubMed ID: 7951259 [No Abstract] [Full Text] [Related]
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52. Clinical application of DNA analysis in a family with OTC deficiency. McClead RE; Rozen R; Fox J; Rosenberg L; Menke J; Bickers R; Morrow G Am J Med Genet; 1986 Nov; 25(3):513-8. PubMed ID: 2878615 [TBL] [Abstract][Full Text] [Related]
53. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis. Brusilow SW J Clin Invest; 1984 Dec; 74(6):2144-8. PubMed ID: 6511918 [TBL] [Abstract][Full Text] [Related]