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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...
Gorde:
| Egile Nagusiak: | , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
American Society of Nephrology
2009
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| Gaiak: | |
| Sarrera elektronikoa: | 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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