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Translating genetic findings in hereditary nephrotic syndrome: the missing loops
Nephrotic syndrome (NS) is a clinicopathological entity characterized by proteinuria, hypoalbuminemia, peripheral edema, and hyperlipidemia. It is the most common cause of glomerular disease in children and adults. Although the molecular pathogenesis of NS is not completely understood, data from the...
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| Yayımlandı: | Am J Physiol Renal Physiol |
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| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
American Physiological Society
2015
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4490379/ https://ncbi.nlm.nih.gov/pubmed/25810439 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajprenal.00683.2014 |
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