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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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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society of Nephrology
2008
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| Matèries: | |
| Accés en línia: | 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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