Title : Hereditary tyrosinemia type I--an overview.

Pub. Date : 1986

PMID : 3296130






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 The primary enzyme defect is a deficiency of fumarylacetoacetase (FAH) (EC 3.7.1.2), the last enzyme in the degradation of tyrosine. Tyrosine fumarylacetoacetate hydrolase Homo sapiens
2 The primary enzyme defect is a deficiency of fumarylacetoacetase (FAH) (EC 3.7.1.2), the last enzyme in the degradation of tyrosine. Tyrosine fumarylacetoacetate hydrolase Homo sapiens