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SCN1B gene variants in Brugada Syndrome: a study of 145 SCN5A-negative patients
Brugada syndrome is characterised by a typical ECG with ST segment elevation in the right precordial leads. Individuals with this condition are susceptible to ventricular arrhythmias and sudden cardiac death. The principal gene responsible for this syndrome is SCN5A, which encodes the α-subunit of t...
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| 出版年: | Sci Rep |
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| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group
2014
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5377327/ https://ncbi.nlm.nih.gov/pubmed/25253298 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep06470 |
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