Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3 -specific calmodulinopathy-Reference-Cited by-同舟云学术

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Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3 -specific calmodulinopathy

Published:2016-05 Issue:3 Volume:2 Page:250-254
ISSN:2214-0271
Container-title:HeartRhythm Case Reports
language:en
Short-container-title:HeartRhythm Case Reports

Author:

Chaix Marie-A.,Koopmann Tamara T.,Goyette Philippe,Alikashani Azadeh,Latour Frédéric,Fatah Meena,Hamilton Robert M.,Rioux John D.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference14 articles.

1. The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy;Schwartz;Eur Heart J,2013

2. Genetic and clinical advances in congenital long QT syndrome;Mizusawa;Circulation J,2014

3. Calmodulin mutations associated with recurrent cardiac arrest in infants;Crotti;Circulation,2013

4. Novel calmodulin mutations associated with congenital arrhythmia susceptibility;Makita;Circ Cardiovasc Genet,2014

5. CALM3 mutation associated with long QT syndrome;Reed;Heart Rhythm,2015

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1. Divergent Biochemical Properties and Disparate Impact of Arrhythmogenic Calmodulin Mutations on Zebrafish Cardiac Function;Journal of Cellular Biochemistry;2024-06-30

2. Long QT syndrome‐associated calmodulin variants disrupt the activity of the slowly activating delayed rectifier potassium channel;The Journal of Physiology;2023-07-10

3. Calmodulin Mutations in Human Disease;Channels;2023-01-11

4. Precision medicine for long QT syndrome: patient-specific iPSCs take the lead;Expert Reviews in Molecular Medicine;2023

5. Calmodulin variant E140G associated with long QT syndrome impairs CaMKIIδ autophosphorylation and L-type calcium channel inactivation;Journal of Biological Chemistry;2023-01

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