Characterization of Loss-Of-Function
Andersen-Tawil syndrome
KCNJ2 variants
Kir2.1 channel
Pierre Robin sequence
catecholaminergic polymorphic ventricular tachycardia
functionnal characterization
Journal
Frontiers in genetics
ISSN: 1664-8021
Titre abrégé: Front Genet
Pays: Switzerland
ID NLM: 101560621
Informations de publication
Date de publication:
2021
2021
Historique:
received:
09
09
2021
accepted:
03
11
2021
entrez:
13
12
2021
pubmed:
14
12
2021
medline:
14
12
2021
Statut:
epublish
Résumé
Andersen-Tawil Syndrome (ATS) is a rare disease defined by the association of cardiac arrhythmias, periodic paralysis and dysmorphic features, and is caused by
Identifiants
pubmed: 34899860
doi: 10.3389/fgene.2021.773177
pii: 773177
pmc: PMC8655864
doi:
Types de publication
Journal Article
Langues
eng
Pagination
773177Informations de copyright
Copyright © 2021 Le Tanno, Folacci, Revilloud, Faivre, Laurent, Pinson, Amedro, Millat, Janin, Vivaudou, Roux-Buisson and Fauré.
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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