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Cardiac conduction defects and Brugada syndrome: A family with overlap syndrome carrying a nonsense SCN5A mutation()

BACKGROUND: Phenotypes often differ even within family members carrying the same SCN5A mutation. We aimed to evaluate the genetic modifiers in a family with Brugada syndrome (BrS) and sick sinus syndrome (SSS) with an SCN5A mutation that causes the truncated alpha-subunit of cardiac Na channel prote...

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發表在:J Arrhythm
Main Authors: Aoki, Hisaaki, Nakamura, Yoshihide, Ohno, Seiko, Makiyama, Takeru, Horie, Minoru
格式: Artigo
語言:Inglês
出版: Elsevier 2017
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC5300865/
https://ncbi.nlm.nih.gov/pubmed/28217227
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.joa.2016.05.007
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