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The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance
For the last 10 years, applying new sequencing technologies to thousands of whole exomes has revealed the high variability of the human genome. Extreme caution should thus be taken to avoid misinterpretation when associating rare genetic variants to disease susceptibility. The Brugada syndrome (BrS)...
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| 出版年: | Front Cardiovasc Med |
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| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Frontiers Media S.A.
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4842929/ https://ncbi.nlm.nih.gov/pubmed/27200363 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcvm.2016.00009 |
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