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Patients with ACTN4 Mutations Demonstrate Distinctive Features of Glomerular Injury
Mutations in ACTN4, the gene encoding the actin-binding protein α-actinin-4, are a cause of familial FSGS. We examined kidney biopsies from patients with ACTN4 mutations to characterize systematically the histopathology of kidney damage in these patients and to determine whether distinctive morpholo...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Nephrology
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3657996/ https://ncbi.nlm.nih.gov/pubmed/19357256 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2008060613 |
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