A New Locus for Familial FSGS on Chromosome 2P

FSGS is a clinicopathologic entity characterized by nephrotic syndrome and progression to ESRD. Although the pathogenesis is unknown, the podocyte seems to play a central role in this disorder. Here, we present six kindreds with hereditary FSGS that did not associate with mutations in known causal g...

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Detalhes bibliográficos
Main Authors: Gbadegesin, Rasheed, Lavin, Peter, Janssens, Louis, Bartkowiak, Bartlomiej, Homstad, Alison, Wu, Guanghong, Bowling, Brandy, Eckel, Jason, Potocky, Chris, Abbott, Diana, Conlon, Peter, Scott, William K., Howell, David, Hauser, Elizabeth, Winn, Michelle P.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2010
Assuntos:
Clinical Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2938593/
https://ncbi.nlm.nih.gov/pubmed/20616172
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2009101046
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