Functional Characterization of Rare Variants in the
Shox2
arrhythmias
atrial fibrillation
cardiac conduction system
pacemaker
sinus node dysfunction
transcription factor
Journal
Frontiers in genetics
ISSN: 1664-8021
Titre abrégé: Front Genet
Pays: Switzerland
ID NLM: 101560621
Informations de publication
Date de publication:
2019
2019
Historique:
received:
04
04
2019
accepted:
19
06
2019
entrez:
30
7
2019
pubmed:
30
7
2019
medline:
30
7
2019
Statut:
epublish
Résumé
Sinus node dysfunction (SND) and atrial fibrillation (AF) often coexist; however, the molecular mechanisms linking both conditions remain elusive. Mutations in the homeobox-containing
Identifiants
pubmed: 31354791
doi: 10.3389/fgene.2019.00648
pmc: PMC6637028
doi:
Types de publication
Journal Article
Langues
eng
Pagination
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