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Molecular Diagnostics in Autosomal Dominant Polycystic Kidney Disease: Utility and Limitations
Background and objectives: Gene-based mutation screening is now available and has the potential to provide diagnostic confirmation or exclusion of autosomal dominant polycystic kidney disease. This study illustrates its utility and limitations in the clinical setting. Design, setting, participants,...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society of Nephrology
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2390981/ https://ncbi.nlm.nih.gov/pubmed/18077784 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.03430807 |
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