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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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Autori principali: Zhao, Xiao, Paterson, Andrew D., Zahirieh, Alireza, He, Ning, Wang, Kairong, Pei, York
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society of Nephrology 2008
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Accesso online: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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