Rare loss-of-function variants in matrisome genes are enriched in Ebstein’s anomaly

Autor: Zhou Zhou, Xia Tang, Wen Chen, Qianlong Chen, Bo Ye, Angad S. Johar, Iftikhar J. Kullo, Keyue Ding
Jazyk: angličtina
Rok vydání: 2024
Předmět:
Zdroj: HGG Advances, Vol 5, Iss 1, Pp 100258- (2024)
Druh dokumentu: article
ISSN: 2666-2477
DOI: 10.1016/j.xhgg.2023.100258
Popis: Summary: Ebstein’s anomaly, a rare congenital heart disease, is distinguished by the failure of embryological delamination of the tricuspid valve leaflets from the underlying primitive right ventricle myocardium. Gaining insight into the genetic basis of Ebstein’s anomaly allows a more precise definition of its pathogenesis. In this study, two distinct cohorts from the Chinese Han population were included: a case-control cohort consisting of 82 unrelated cases and 125 controls without cardiac phenotypes and a trio cohort comprising 36 parent-offspring trios. Whole-exome sequencing data from all 315 participants were utilized to identify qualifying variants, encompassing rare (minor allele frequency
Databáze: Directory of Open Access Journals