St-Louis, M <br/><br/>
Mutations in the fumarylacetoacetate hydrolase gene causing hereditary tyrosinemia type I: overview.  [electronic resource] 

 -  Human mutation  1997 
 - 291-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1059-7794 
<br/><br/><label>Standard No.: </label>10.1002/(SICI)1098-1004(1997)9:4<291::AID-HUMU1>3.0.CO;2-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Metabolism, Inborn Errors--genetics<br/>Animals<br/>Disease Models, Animal<br/>Humans<br/>Hydrolases--genetics<br/>Mice<br/>Mutation--genetics<br/>Tyrosine--metabolism