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 a-subunit of the cardiac sodium channel. Typically, BrS mutations in SCN5A result in a reduction of sodium current with some mutations even exhibiting a...
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| Main Authors: | , , , , , , , |
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| Format: | Journal |
| Published: |
2018
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| Online Access: | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84903591807&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/45522 |
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| Institution: | Chiang Mai University |