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Biochem Med Metab Biol. 1992 Aug;48(1):26-31.

Nucleotide sequence of a cDNA encoding murine fumarylacetoacetate hydrolase.

Author information

1
Department of Molecular and Medical Genetics, Oregon Health Sciences University, Portland 97201.

Abstract

Hereditary tyrosinemia type I is caused by deficiency of the enzyme fumarylacetoacetate hydrolase (FAH) (EC 3.7.1.2), the final step in tyrosine degradation. We report here the cloning and sequencing of a full length cDNA coding for murine FAH. This cDNA is highly homologous to the previously cloned human and rat genes.

PMID:
1524868
[Indexed for MEDLINE]

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