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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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| Asıl Yazarlar: | , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2010
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| 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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