NPHS2 Variation in Sporadic Focal Segmental Glomerulosclerosis

Mutations in NPHS2, the gene that encodes podocin, are well-established causes of both familial and sporadic steroid-resistant focal segmental glomerulosclerosis (FSGS) in the pediatric population, but have not been well-characterized in late-onset disease. To investigate the role of NPHS2 polymorph...

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主要な著者: McKenzie, Louise M., Hendrickson, Sher L., Briggs, William A., Dart, Richard A., Korbet, Stephen M., Mokrzycki, Michelle H., Kimmel, Paul L., Ahuja, Tejinder S., Berns, Jeffrey S., Simon, Eric E., Smith, Michael C., Trachtman, Howard, Michel, Donna M., Schelling, Jeffrey R., Cho, Monique, Zhou, Yu C., Binns-Roemer, Elizabeth, Kirk, Gregory D., Kopp, Jeffrey B., Winkler, Cheryl A.
フォーマット: Artigo
言語:Inglês
出版事項: 2007
主題:
Article
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4096868/
https://ncbi.nlm.nih.gov/pubmed/17942957
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2007030319
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