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Article

A method of identifying the high-risk mutations of sudden cardiac death at KCNQ1 and KCNH2 genes.

Journal of forensic and legal medicine - 1 Jul 2024

Wang Jiaqi, Liu Zidong, Zhang Yuxin, Zhang Mingming, Chen Deqing, Zhang Gengqian

Abstract excerpt

Sudden Cardiac Death (SCD) often shows negative anatomy results after a systemic autopsy and the gene mutations of potassium channel play a key role in the etiology of SCD. We established a feasible system to detect SCD-related mutations and investigated the mutations at KCNQ1 and KCNH2 genes in the Chinese population. We established a mutation detection system combined with multiplex PCR, SNaPshot technique, and...

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Source

Identifiers

PMID: 38908219
DOI: 10.1016/j.jflm.2024.102707

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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