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A Mutation in the S3 Segment of KCNQ1 Results in Familial Lone Atrial Fibrillation
BACKGROUND: Mutations in several ion channel genes have been reported to cause rare cases of familial atrial fibrillation (AF). OBJECTIVE: We sought to determine the genetic basis for AF in a family with autosomal dominant AF. METHODS AND RESULTS: Family members were evaluated by 12-lead ECG, echoca...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3038671/ https://ncbi.nlm.nih.gov/pubmed/19632626 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2009.04.015 |
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