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- W2091235861 abstract "Purpose of review In this article, we summarize the main features of the most common inherited channelopathies, focusing on the findings that advanced the field in the last few years. Recent findings The progress in genetics prompted the discovery of several new genes associated with ion-channel disorders, elucidating new molecular pathways and new arrhythmogenic mechanisms. The diffusion and availability of genetic screening gave a new relevance to the application of genetics not only for diagnosis, but also for risk assessment and therapeutic decisions. As a consequence, the present challenge in the field is represented by the need to use genetic data to develop personalized clinical approaches. Summary Over a few years, the field of inherited arrhythmogenic diseases has rapidly expanded, thus reshaping clinical management for these conditions. It is now clear that to handle these patients a specialized expertise is needed, able to translate the discoveries derived from basic science studies into the clinical care of the patients." @default.
- W2091235861 created "2016-06-24" @default.
- W2091235861 creator A5008966758 @default.
- W2091235861 creator A5021196395 @default.
- W2091235861 creator A5033233937 @default.
- W2091235861 date "2012-05-01" @default.
- W2091235861 modified "2023-10-07" @default.
- W2091235861 title "Genetics of ion-channel disorders" @default.
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- W2091235861 doi "https://doi.org/10.1097/hco.0b013e328352429d" @default.
- W2091235861 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22450718" @default.