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
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

773177

Informations 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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Auteurs

Pauline Le Tanno (P)

Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France.

Mathilde Folacci (M)

CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France.

Jean Revilloud (J)

CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France.

Laurence Faivre (L)

Medical Genetics Department, Dijon Bourgogne University Hospital, François Mitterand Hospital, Dijon, France.

Gabriel Laurent (G)

Cardiology Department, Dijon Bourgogne University Hospital, François Mitterand Hospital, Dijon, France.

Lucile Pinson (L)

Medical Genetics Department, University Hospital, Montpellier, France.
Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Montpellier, France.
Genetic Department for Rare Diseases and Personalized Medicine, Clinical Division, Montpellier, France.

Pascal Amedro (P)

Pediatric and Congenital Cardiology Department, Clinical Investigation Centre, PhyMedExp, CNRS, INSERM, University of Montpellier, University Hospital, Montpellier, France.

Gilles Millat (G)

Laboratoire de Cardiogénétique Moléculaire, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon, Lyon, France.

Alexandre Janin (A)

Laboratoire de Cardiogénétique Moléculaire, Centre de Biologie et Pathologie Est, Hospices Civils de Lyon, Lyon, France.

Michel Vivaudou (M)

CEA, CNRS, Institut de Biologie Structurale, Université Grenoble Alpes, Grenoble, France.

Nathalie Roux-Buisson (N)

Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France.

Julien Fauré (J)

Université Grenoble Alpes, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, Grenoble, France.

Classifications MeSH