Harambat, Jérôme <br/><br/>
Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome.  [electronic resource] 

 -  Kidney international  Mar 2010 
 - 443-9 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1523-1755 
<br/><br/><label>Standard No.: </label>10.1038/ki.2009.435  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Arginine--metabolism<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Genotype<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Hyperoxaluria, Primary--diagnosis<br/>Infant<br/>Kidney Failure, Chronic--genetics<br/>Mutation<br/>Phenotype<br/>Prognosis<br/>Retrospective Studies<br/>Transaminases--genetics