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: | Article |
| Language: | English |
| Published: |
Lippincott Williams and Wilkins
2014
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| Online Access: | http://www.scopus.com/inward/record.url?eid=2-s2.0-84903591807&partnerID=40&md5=32ba9855444be129f744295afc2d5800 http://cmuir.cmu.ac.th/handle/6653943832/1787 |
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| Institution: | Chiang Mai University |
| Language: | English |