A Novel Missense Mutation of Wilms’ Tumor 1 Causes Autosomal Dominant FSGS

FSGS is a clinical disorder characterized by focal scarring of the glomerular capillary tuft, podocyte injury, and nephrotic syndrome. Although idiopathic forms of FSGS predominate, recent insights into the molecular and genetic causes of FSGS have enhanced our understanding of disease pathogenesis....

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Vydáno v:J Am Soc Nephrol
Hlavní autoři: Hall, Gentzon, Gbadegesin, Rasheed A., Lavin, Peter, Wu, Guanghong, Liu, Yangfan, Oh, Edwin C., Wang, Liming, Spurney, Robert F., Eckel, Jason, Lindsey, Thomas, Homstad, Alison, Malone, Andrew F., Phelan, Paul J., Shaw, Andrey, Howell, David N., Conlon, Peter J., Katsanis, Nicholas, Winn, Michelle P.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society of Nephrology 2015
Témata:
Basic Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4378093/
https://ncbi.nlm.nih.gov/pubmed/25145932
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2013101053
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