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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Päätekijät: Das, Saumya, Makino, Seiko, Melman, Yonathan F., Shea, Marisa A., Goyal, Sanjeev B., Rosenzweig, Anthony, MacRae, Calum A., Ellinor, Patrick T.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2009
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Linkit: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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