New Family With Catecholaminergic Polymorphic Ventricular Tachycardia Linked to the Triadin Gene-Reference-Cited by-同舟云学术

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New Family With Catecholaminergic Polymorphic Ventricular Tachycardia Linked to the Triadin Gene

Published:2015-09-01 Issue:10 Volume:26 Page:1146-1150
ISSN:1045-3873
Container-title:Journal of Cardiovascular Electrophysiology
language:en
Short-container-title:J Cardiovasc Electrophysiol

Author:

ROORYCK CAROLINE¹²³,KYNDT FLORENCE⁴,BOZON DOMINIQUE⁵,ROUX-BUISSON NATHALIE⁶,SACHER FREDERIC²,PROBST VINCENT⁴,THAMBO JEAN-BENOIT²³

Affiliation:

1. Univ. Bordeaux; Maladies Rares: Génétique et Métabolisme (MRGM); Bordeaux France

2. LIRYC, L'Institut de rythmologie et modélisation cardiaque; Université de Bordeaux INSERM; France

3. Service des cardiopathies congénitales; Hôpital Cardiologique du Haut-Lévêque; CHU Bordeaux; Bordeaux France

4. Institut du thorax, Clinique Cardiologique Inserm; CHU de Nantes; France

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

6. INSERM U836, Grenoble Institut des Neurosciences; Equipe Muscle et Pathologies; Grenoble France

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jce.12763/fullpdf

Reference11 articles.

1. Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death;Nyegaard;Am J Hum Genet,2012

2. Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human;Roux-Buisson;Hum Mol Genet,2012

3. Splicing in action: Assessing disease causing sequence changes;Baralle;J Med Genet,2005

4. U1 snRNA mis-binding: A new cause of CMT1B;Crehalet;Neurogenetics,2010

5. A novel approach to describe a U1 snRNA binding site;Freund;Nucleic Acids Res,2003

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1. Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes;Stem Cell Reports;2023-05

2. CPVT and Complete Atrio-Ventricular Block: The Flipside of the Same Coin;Journal of Cardiovascular Development and Disease;2023-02-23

3. Calcium Handling in Inherited Cardiac Diseases: A Focus on Catecholaminergic Polymorphic Ventricular Tachycardia and Hypertrophic Cardiomyopathy;International Journal of Molecular Sciences;2023-02-08

4. A very rare cause of sudden cardiac arrest in children: triadin knockout syndrome;Cardiology in the Young;2022-04-28

5. An Optogenetic Arrhythmia Model—Insertion of Several Catecholaminergic Polymorphic Ventricular Tachycardia Mutations Into Caenorhabditis elegans UNC-68 Disturbs Calstabin-Mediated Stabilization of the Ryanodine Receptor Homolog;Frontiers in Physiology;2022-03-25

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