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Novel Mutation in the KCNJ2 Gene Is Associated with a Malignant Arrhythmic Phenotype of Andersen‐Tawil Syndrome

BACKGROUND: Andersen‐Tawil syndrome (ATS) is a rare inherited multisystem disorder associated with mutations in KCNJ2 and low prevalence of life‐threatening ventricular arrhythmias. Our aim was to describe the clinical course of ATS in a family, in which the proband survived aborted cardiac arrest (...

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Detalhes bibliográficos
Publicado no:Ann Noninvasive Electrocardiol
Main Authors: Fernlund, E., Lundin, C., Hertervig, E., Kongstad, O., Alders, M., Platonov, P.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6932293/
https://ncbi.nlm.nih.gov/pubmed/24047492
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/anec.12074
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