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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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| Опубликовано в: : | Pediatr Nephrol |
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| Главные авторы: | , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2014
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| Предметы: | |
| Online-ссылка: | 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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