Williams, Emma L <br/><br/>
Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT gene.  [electronic resource] 

 -  Human mutation  Jun 2009 
 - 910-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Review 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.21021  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Animals<br/>DNA Mutational Analysis<br/>Humans<br/>Hyperoxaluria, Primary--diagnosis<br/>Polymorphism, Genetic<br/>Transaminases--chemistry<br/>Uniparental Disomy--genetics