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Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?
Brugada syndrome is a rare inherited arrhythmogenic disease leading to ventricular fibrillation and high risk of sudden death. In 1998, this syndrome was linked with a genetic variant with an autosomal dominant pattern of inheritance. To date, rare variants identified in more than 40 genes have been...
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| Veröffentlicht in: | Int J Mol Sci |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
MDPI
2020
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7582739/ https://ncbi.nlm.nih.gov/pubmed/32998306 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21197155 |
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