Title : Mutations in the fumarylacetoacetate hydrolase gene causing hereditary tyrosinemia type I: overview.

Pub. Date : 1997

PMID : 9101289






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Tyrosinemia type I is an inborn error of metabolism caused by a deficiency in the last enzyme of the tyrosine catabolic pathway, fumarylacetoacetate hydrolase (FAH). Tyrosine fumarylacetoacetate hydrolase Homo sapiens
2 Tyrosinemia type I is an inborn error of metabolism caused by a deficiency in the last enzyme of the tyrosine catabolic pathway, fumarylacetoacetate hydrolase (FAH). Tyrosine fumarylacetoacetate hydrolase Homo sapiens