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5. Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I). Tanguay RM, Valet JP, Lescault A, Duband JL, Laberge C, Lettre F, Plante M. Am J Hum Genet; 1990 Aug; 47(2):308-16. PubMed ID: 2378356 [Abstract] [Full Text] [Related]
6. Type 1 hereditary tyrosinemia. Evidence for molecular heterogeneity and identification of a causal mutation in a French Canadian patient. Phaneuf D, Lambert M, Laframboise R, Mitchell G, Lettre F, Tanguay RM. J Clin Invest; 1992 Oct; 90(4):1185-92. PubMed ID: 1401056 [Abstract] [Full Text] [Related]
8. Nucleotide sequence of a cDNA encoding murine fumarylacetoacetate hydrolase. Grompe M, al-Dhalimy M. Biochem Med Metab Biol; 1992 Aug; 48(1):26-31. PubMed ID: 1524868 [Abstract] [Full Text] [Related]
9. Purification of mRNA coding for the enzyme deficient in hereditary tyrosinemia, fumarylacetoacetate hydrolase. Nicole LM, Valet JP, Laberge C, Tanguay RM. Biochem Cell Biol; 1986 May; 64(5):489-93. PubMed ID: 3718716 [Abstract] [Full Text] [Related]
10. Localization of cells in the rat brain expressing fumarylacetoacetate hydrolase, the deficient enzyme in hereditary tyrosinemia type 1. Labelle Y, Puymirat J, Tanguay RM. Biochim Biophys Acta; 1993 Jan 22; 1180(3):250-6. PubMed ID: 8422430 [Abstract] [Full Text] [Related]
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17. Structural and functional analysis of missense mutations in fumarylacetoacetate hydrolase, the gene deficient in hereditary tyrosinemia type 1. Bergeron A, D'Astous M, Timm DE, Tanguay RM. J Biol Chem; 2001 May 04; 276(18):15225-31. PubMed ID: 11278491 [Abstract] [Full Text] [Related]
19. Fumarylacetoacetate Hydrolase Knock-out Rabbit Model for Hereditary Tyrosinemia Type 1. Li L, Zhang Q, Yang H, Zou Q, Lai C, Jiang F, Zhao P, Luo Z, Yang J, Chen Q, Wang Y, Newsome PN, Frampton J, Maxwell PH, Li W, Chen S, Wang D, Siu TS, Tam S, Tse HF, Qin B, Bao X, Esteban MA, Lai L. J Biol Chem; 2017 Mar 17; 292(11):4755-4763. PubMed ID: 28053091 [Abstract] [Full Text] [Related]