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Article

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

Journal of Zhejiang University. Science. B - 1 Jul 2005

Shang Yun-peng, Xie Xu-dong, Wang Xing-xiang, Chen Jun-zhu, Zhu Jian-hua, Tao Qian-min, Zheng Liang-rong

Abstract excerpt

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 underlying genetic basis of a Chinese family with LQTS and to characterize the clinical manifestations properties of the...

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Source

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Identifiers

PMID: 15973763
DOI: 10.1631/jzus.2005.B0626
PMCID: PMC1389795

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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