Cargando…
Arrhythmogenic Cardiomyopathy in a Patient With a Rare Loss‐of‐Function KCNQ1 Mutation
BACKGROUND: Ventricular tachycardia (VT) is a common manifestation of advanced cardiomyopathies. In a subset of patients with dilated cardiomyopathy, VT is the initial and the cardinal manifestation of the disease. The molecular genetic basis of this subset of dilated cardiomyopathy is largely unkno...
Autores principales: | Xiong, Qinmei, Cao, Qing, Zhou, Qiongqiong, Xie, Jinyan, Shen, Yang, Wan, Rong, Yu, Jianhua, Yan, Sujuan, Marian, Ali J., Hong, Kui |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4330077/ https://www.ncbi.nlm.nih.gov/pubmed/25616976 http://dx.doi.org/10.1161/JAHA.114.001526 |
Ejemplares similares
-
Genotype-phenotype relationship in patients with arrhythmogenic right ventricular cardiomyopathy caused by desmosomal gene mutations: A systematic review and meta-analysis
por: Xu, Zhenyan, et al.
Publicado: (2017) -
A Rare Loss-of-Function SCN5A Variant is Associated With Lidocaine-induced Ventricular Fibrillation
por: Xiong, Qinmei, et al.
Publicado: (2014) -
Arrhythmogenic cardiomyopathy
por: Pilichou, Kalliopi, et al.
Publicado: (2016) -
Desmin Mutations and Arrhythmogenic Right Ventricular Cardiomyopathy
por: Lorenzon, Alessandra, et al.
Publicado: (2013) -
Identification of established arrhythmogenic right ventricular cardiomyopathy mutation in a patient with the contrasting phenotype of hypertrophic cardiomyopathy
por: Bainbridge, Matthew Neil, et al.
Publicado: (2017)