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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Detalhes bibliográficos
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Article
Acesso em linha: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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