St-Louis, M <br/><br/>
Simple detection of a (Finnish) hereditary tyrosinemia type 1 mutation.  [electronic resource] 

 -  Human mutation  1996 
 - 379-80 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1059-7794 
<br/><br/><label>Standard No.: </label>10.1002/(SICI)1098-1004(1996)7:4<379::AID-HUMU20>3.0.CO;2-Z  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Metabolism, Inborn Errors--ethnology<br/>Base Sequence<br/>DNA Primers<br/>Finland<br/>Genetic Carrier Screening<br/>Heterozygote<br/>Humans<br/>Molecular Sequence Data<br/>Mutation<br/>Tyrosine--blood