Title : Deficient DNA-ligase activity in the metabolic disease tyrosinemia type I.

Pub. Date : 1998 Oct 13

PMID : 9770534






1 Functional Relationships(s)
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1 Hereditary tyrosinemia type I (HT1) is an autosomal recessive inborn error of metabolism caused by the deficiency of fumarylacetoacetate hydrolase, the last enzyme in the tyrosine catabolism pathway. Tyrosine fumarylacetoacetate hydrolase Homo sapiens