Cargando…
A mutation in the CACNA1C gene leads to early repolarization syndrome with incomplete penetrance: A Chinese family study
BACKGROUND: Early repolarization syndrome (ERS) may be a near-Mendelian or an oligogenic disease; however, no direct evidence has been provided to support this theory. METHODS AND RESULTS: We described a large Chinese family with nocturnal sudden cardiac death induced by ERS in most of the young mal...
Autores principales: | Liu, Xin, Shen, Yang, Xie, Jinyan, Bao, Huihui, Cao, Qing, Wan, Rong, Xu, Xiaoming, Zhou, Hui, Huang, Lin, Xu, Zhenyan, Zhu, Wengen, Hu, Jinzhu, Cheng, Xiaoshu, Hong, Kui |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5426766/ https://www.ncbi.nlm.nih.gov/pubmed/28493952 http://dx.doi.org/10.1371/journal.pone.0177532 |
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) -
Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome
por: Chen, Yanhong, et al.
Publicado: (2017) -
Relation of Body Mass Index With Adverse Outcomes Among Patients With Atrial Fibrillation: A Meta‐Analysis and Systematic Review
por: Zhu, Wengen, et al.
Publicado: (2016) -
Association of single nucleotide polymorphisms in CACNA 1A/CACNA 1C/CACNA 1H calcium channel genes with diabetic peripheral neuropathy in Chinese population
por: Sun, Lin, et al.
Publicado: (2018) -
Low arterial oxygen partial pressure induces pulmonary thrombocytopenia in patients and a mouse model
por: Wu, Limeng, et al.
Publicado: (2021)