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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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| Publicado no: | J Am Soc Nephrol |
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| Main Authors: | , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Nephrology
2015
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| Assuntos: | |
| Acesso em linha: | 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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