Title : Tyrosinaemia type I--an update.

Pub. Date : 1991

PMID : 1749221






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Tyrosinaemia type I is a recessively inherited disorder caused by a deficiency of fumarylacetoacetase (FAH), the last enzyme in tyrosine degradation. Tyrosine fumarylacetoacetate hydrolase Homo sapiens
2 Tyrosinaemia type I is a recessively inherited disorder caused by a deficiency of fumarylacetoacetase (FAH), the last enzyme in tyrosine degradation. Tyrosine fumarylacetoacetate hydrolase Homo sapiens