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Article

TBX20 loss-of-function mutation associated with familial dilated cardiomyopathy.

Clinical chemistry and laboratory medicine - 1 Feb 2016

Zhao Cui-Mei, Bing-Sun, Song Hao-Ming, Wang Juan, Xu Wen-Jun, Jiang Jin-Fa, Qiu Xing-Biao, Yuan Fang, Xu Jia-Hong, Yang Yi-Qing

Abstract excerpt

BACKGROUND: Dilated cardiomyopathy (DCM) is a major cause of congestive heart failure, sudden cardiac death and cardiac transplantation. Aggregating evidence highlights the genetic origin of DCM. However, DCM is a genetically heterogeneous disorder, and the genetic components underlying DCM in most cases remain unknown. METHODS: The coding regions and splicing junction sites of the TBX20 gene were sequenced in...

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Source

Identifiers

PMID: 26118961
DOI: 10.1515/cclm-2015-0328

Genes

TBX20
GATA4

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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