Novel
Brugada syndrome
SCN5A
arrhythmia
atrial fibrillation
genetic testing
mutation
sodium channel
sudden cardiac death
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:
30
07
2018
accepted:
23
05
2019
entrez:
25
6
2019
pubmed:
25
6
2019
medline:
25
6
2019
Statut:
epublish
Résumé
In this case report, we characterize a novel inherited frameshift mutation c.4700_4701del (p.Phe1567Cysfs
Identifiants
pubmed: 31231430
doi: 10.3389/fgene.2019.00547
pmc: PMC6565861
doi:
Types de publication
Journal Article
Langues
eng
Pagination
547Références
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