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Partially dominant mutant channel defect corresponding with intermediate Long-QT2 phenotype
BACKGROUND: The hereditary Long QT Syndrome (LQTS) is a common cardiac disorder where ventricular repolarization is delayed, abnormally prolonging the QTc interval on ECG. LQTS is linked to various genetic loci including the KCNH2 (HERG) gene that encodes the α–subunit of the cardiac potassium chann...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3248989/ https://ncbi.nlm.nih.gov/pubmed/21951015 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1540-8159.2011.03222.x |
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