Long Noncoding RNA
22q11.2 deletion
Wnt/β-catenin signaling
congenital heart disease
lnc-TSSK2-8
long noncoding RNA
Journal
Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250
Informations de publication
Date de publication:
2021
2021
Historique:
received:
29
01
2021
accepted:
29
03
2021
entrez:
27
5
2021
pubmed:
28
5
2021
medline:
28
5
2021
Statut:
epublish
Résumé
Congenital heart defects (CHDs) are the most common birth defects worldwide. 22q11.2 deletion syndrome is the most common microdeletion disorder that has been frequently associated with conotruncal malformations. By now, the dosage-sensitive gene
Identifiants
pubmed: 34041241
doi: 10.3389/fcell.2021.660576
pmc: PMC8141806
doi:
Types de publication
Journal Article
Langues
eng
Pagination
660576Informations de copyright
Copyright © 2021 Fa, Zhang, Zhang, Qi, Zhang, Fu, Xu, Gao and Wang.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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