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KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties
BACKGROUND: Loss-of-function mutations in the KCNJ2 cause ~50% of Andersen-Tawil Syndrome (ATS) characterized by a classic triad of periodic paralysis, ventricular arrhythmia, and dysmorphic features. Do KCNJ2 mutations occur in patients lacking this triad and lacking a family history of ATS? OBJECT...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1868697/ https://ncbi.nlm.nih.gov/pubmed/17341397 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2006.10.025 |
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