The association of podocin R229Q polymorphism with increased albuminuria or reduced estimated GFR in a large population-based sample of U.S. adults

BACKGROUND: Rare mutations in nephrosis 2 (NPHS2), encoding podocin, are found in patients with familial and sporadic steroid resistant nephrotic syndrome and focal segmental glomerular sclerosis. The objective of this study was to assess the contribution of the commonly reported functional podocin...

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Hoofdauteurs: Köttgen, Anna, Hsu, Charles C., Coresh, Josef, Shuldiner, Alan R., Berthier-Schaad, Yvette, Gambhir, Tejal Rami, Smith, Michael W., Boerwinkle, Eric, Kao, W. H. Linda
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2008
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2597304/
https://ncbi.nlm.nih.gov/pubmed/18499321
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1053/j.ajkd.2008.02.306
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