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Short QT syndrome Genotype-phenotype correlations
The short QT syndrome is a new congenital entity associated with familial atrial fibrillation and/or sudden death or syncope. Three different gain-of-function mutations in genes encoding for cardiac potassium channels (KCNH2, KCNQ1, and KCNJ2) have been identified up to now to cause short QT syndrom...
Tallennettuna:
| Päätekijät: | , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2005
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1474068/ https://ncbi.nlm.nih.gov/pubmed/16226079 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jelectrocard.2005.06.009 |
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