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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書誌詳細
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: 2008
主題:
Article
オンライン･アクセス: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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