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Genetic causes of proteinuria and nephrotic syndrome: Impact on podocyte pathobiology
In the past 20 years, multiple genetic mutations have been identified in patients with congenital nephrotic syndrome (CNS) and both familial and sporadic focal segmental glomerulosclerosis (FSGS). Characterization of the genetic basis of CNS and FSGS has led to the recognition of the importance of p...
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| Yayımlandı: | Pediatr Nephrol |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2014
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4262721/ https://ncbi.nlm.nih.gov/pubmed/24584664 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00467-014-2753-3 |
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