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Article

VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy.

European journal of medical genetics - 1 Mar 2023

Shi Hong-Yu, Xie Meng-Shi, Guo Yu-Han, Yang Chen-Xi, Gu Jia-Ning, Qiao Qi, Di Ruo-Min, Qiu Xing-Biao, Xu Ying-Jia, Yang Yi-Qing

Abstract excerpt

Dilated cardiomyopathy (DCM), characteristic of left ventricular or biventricular dilation with systolic dysfunction, is the most common form of cardiomyopathy, and a leading cause of heart failure and sudden cardiac death. Aggregating evidence highlights the underlying genetic basis of DCM, and mutations in over 100 genes have been causally linked to DCM. Nevertheless, due to pronounced genetic heterogeneity,...

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Identifiers

PMID: 36657711
DOI: 10.1016/j.ejmg.2023.104705

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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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