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

St-Louis, M

Mutations in the fumarylacetoacetate hydrolase gene causing hereditary tyrosinemia type I: overview. [electronic resource] - Human mutation 1997 - 291-9 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review

1059-7794

10.1002/(SICI)1098-1004(1997)9:4<291::AID-HUMU1>3.0.CO;2-9 doi


Amino Acid Metabolism, Inborn Errors--genetics
Animals
Disease Models, Animal
Humans
Hydrolases--genetics
Mice
Mutation--genetics
Tyrosine--metabolism