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Article

ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy.

Heart and vessels - 1 Jul 2018

Sun Yu-Min, Wang Jun, Xu Ying-Jia, Wang Xin-Hua, Yuan Fang, Liu Hua, Li Ruo-Gu, Zhang Min, Li Yan-Jie, Shi Hong-Yu, Zhao Liang, Qiu Xing-Biao, Qu Xin-Kai, Yang Yi-Qing

Abstract excerpt

Dilated cardiomyopathy (DCM) is a common primary myocardial disease leading to congestive heart failure, arrhythmia and sudden cardiac death. Increasing studies demonstrate substantial genetic determinants for DCM. Nevertheless, DCM is of substantial genetic heterogeneity, and the genetic basis for DCM in most patients remains unclear. The present study was sought to investigate the association of a genetic...

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Source

Identifiers

PMID: 29445930
DOI: 10.1007/s00380-017-1110-4

Genes

ZBTB17

Variants

Provenance

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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