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Article

MESP1 Mutations in Patients with Congenital Heart Defects.

Human mutation - 1 Mar 2016

Werner Petra, Latney Brande, Deardorff Matthew A, Goldmuntz Elizabeth

Abstract excerpt

Identifying the genetic etiology of congenital heart disease (CHD) has been challenging despite being one of the most common congenital malformations in humans. We previously identified a microdeletion in a patient with a ventricular septal defect containing over 40 genes including MESP1 (mesoderm posterior basic helix-loop-helix transcription factor 1). Because of the importance of MESP1 as an early regulator of...

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Source

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Identifiers

PMID: 26694203
DOI: 10.1002/humu.22947
PMCID: PMC4762608

Genes

MESP1

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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