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Congenital Long-QT Syndromes: A Clinical and Genetic Update From Infancy Through Adulthood
Long-QT syndromes (LQTSs) have been described in all ages and are a significant cause of cardiovascular mortality, especially in structurally normal hearts. Abnormalities in transmembrane ion conduction channels and structural proteins produce these clinical syndromes, labeled LQT1-LQT12; however, g...
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| Publicado no: | Trends Cardiovasc Med |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4260467/ https://ncbi.nlm.nih.gov/pubmed/19185812 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tcm.2008.11.002 |
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