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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Dades bibliogràfiques
Publicat a:J Am Soc Nephrol
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: American Society of Nephrology 2015
Matèries:
Basic Research
Accés en línia: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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