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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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Detaylı Bibliyografya
Yayımlandı:Pediatr Nephrol
Asıl Yazarlar: Akchurin, Oleh, Reidy, Kimberly J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2014
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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