Title : Hypermethioninemias of genetic and non-genetic origin: A review.

Pub. Date : 2011 Feb 15

PMID : 21308989






1 Functional Relationships(s)
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Protein Name
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1 (6) Fumarylacetoacetate hydrolase (FAH) deficiency (tyrosinemia type I) may lead to hypermethioninemia secondary either to liver damage and/or to accumulation of fumarylacetoacetate, an inhibitor of the high K(m) MAT. fumarylacetoacetate fumarylacetoacetate hydrolase Homo sapiens