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A novel splice mutation of HERG in a Chinese family with long QT syndrome

Congenital long QT syndrome (LQTS) is a genetically heterogeneous disease in which six ion-channel genes have been identified. The phenotype-genotype relationships of the HERG (human ether-a-go-go-related gene) mutations are not fully understood. The objective of this study is to identify the underl...

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Главные авторы: Shang, Yun-peng, Xie, Xu-dong, Wang, Xing-xiang, Chen, Jun-zhu, Zhu, Jian-hua, Tao, Qian-min, Zheng, Liang-rong
Формат: Artigo
Язык:Inglês
Опубликовано: Zhejiang University Press 2005
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Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1389795/
https://ncbi.nlm.nih.gov/pubmed/15973763
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1631/jzus.2005.B0626
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