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Article

Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy.

European journal of medical genetics - 1 Apr 2020

Di Ruo-Min, Yang Chen-Xi, Zhao Cui-Mei, Yuan Fang, Qiao Qi, Gu Jia-Ning, Li Xiu-Mei, Xu Ying-Jia, Yang Yi-Qing

Abstract excerpt

As a prevalent primary myocardial disease, dilated cardiomyopathy (DCM) represents the most common cause of heart failure in the young and the most frequent indication for cardiac transplantation. Aggregating evidence highlights the genetic basis of DCM. However, due to substantial genetic heterogeneity, the genetic defects of DCM in most cases remain elusive. In the current investigation, the entire coding exons...

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PMID: 31857253
DOI: 10.1016/j.ejmg.2019.103827

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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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