Characterization of a Chinese KCNQ1 mutation (R259H) that shortens repolarization and causes short QT syndrome 2

OBJECTIVES: To evaluate the association between a KCNQ1 mutation, R259H, and short QT syndrome (SQTS) and to explore the electrophysiological mechanisms underlying their association. METHODS: We performed genetic screening of SQTS genes in 25 probands and their family members (63 patients). We used...

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Detalles Bibliográficos
Autores principales: Wu, Zhi-Juan, Huang, Yun, Fu, Yi-Cheng, Zhao, Xiao-Jing, Zhu, Chao, Zhang, Yu, Xu, Bin, Zhu, Qing-Lei, Li, Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Science Press 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554793/
https://www.ncbi.nlm.nih.gov/pubmed/26346102
http://dx.doi.org/10.11909/j.issn.1671-5411.2015.04.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554793/
https://www.ncbi.nlm.nih.gov/pubmed/26346102
http://dx.doi.org/10.11909/j.issn.1671-5411.2015.04.002

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