Article

RCAN family member 3 deficiency contributes to noncompaction of the ventricular myocardium

2022-12-14

Abstract excerpt

<title>Abstract</title> <p>Noncompaction of the ventricular myocaridium (NVM), as the third most commonly diagnosed cardiomyopathy, is characterized with highly variable clinical manifestations. Due to high heterogeneity, the genetic etiology of 40–60% NVM cases remains unknown. Here, we reported two infants of NVM in a non-consanguineous family with typically clinical presentation of persistent bradycardia since...

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Literature Corpus work: 10135739-1753-5299-9bd8-e4f238a0abdd
DOI: 10.21203/rs.3.rs-2339970/v1

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