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Molecular diagnostics for autosomal dominant polycystic kidney disease

Autosomal dominant polycystic kidney disease (ADPKD) is a common nephropathy caused by mutations in either PKD1 or PKD2. Mutations in PKD1 account for ~85% of cases and cause more severe disease than mutations in PKD2. Diagnosis of ADPKD before the onset of symptoms is usually performed using renal...

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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Harris, Peter C., Rossetti, Sandro
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2010
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4050432/
https://ncbi.nlm.nih.gov/pubmed/20177400
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nrneph.2010.18
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