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Long QT syndrome: novel insights into the mechanisms of cardiac arrhythmias
The congenital long QT syndrome is a rare disorder in which mutation carriers are at risk for polymorphic ventricular tachycardia and/or sudden cardiac death. Discovery and analysis of gene mutations associated with variants of this disorder have provided novel insight into mechanisms of cardiac arr...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
American Society for Clinical Investigation
2003
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC193679/ https://ncbi.nlm.nih.gov/pubmed/12975462 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200319844 |
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