Tzur, Shay <br/><br/>
Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.  [electronic resource] 

 -  Human genetics  Sep 2010 
 - 345-50 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1432-1203 
<br/><br/><label>Standard No.: </label>10.1007/s00439-010-0861-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Africa<br/>Apolipoprotein L1<br/>Apolipoproteins--genetics<br/>Chromosome Mapping<br/>Genetic Predisposition to Disease<br/>Haplotypes<br/>Humans<br/>Kidney Failure, Chronic--genetics<br/>Linkage Disequilibrium<br/>Lipoproteins, HDL--genetics<br/>Molecular Motor Proteins--genetics<br/>Mutation, Missense<br/>Myosin Heavy Chains--genetics<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Risk Factors