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Brugada Syndrome Disease Phenotype Explained in Apparently Benign Sodium Channel Mutations

BACKGROUND: Brugada syndrome (BrS) is an arrhythmogenic disorder that has been linked to mutations in SCN5A, the gene encoding for the pore-forming α-subunit of the cardiac sodium channel. Typically, BrS mutations in SCN5A result in a reduction of sodium current with some mutations even exhibiting a...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Hoshi, Malcolm, Du, Xi X., Shinlapawittayatorn, Krekwit, Liu, Haiyan, Chai, Sam, Wan, Xiaoping, Ficker, Eckhard, Deschênes, Isabelle
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: 2014
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3989843/
https://ncbi.nlm.nih.gov/pubmed/24573164
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.113.000292
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