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

Detalles Bibliográficos
Autores principales: Chaix, Marie-A., Koopmann, Tamara T., Goyette, Philippe, Alikashani, Azadeh, Latour, Frédéric, Fatah, Meena, Hamilton, Robert M., Rioux, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419757/
https://www.ncbi.nlm.nih.gov/pubmed/28491681
http://dx.doi.org/10.1016/j.hrcr.2016.02.002
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author Chaix, Marie-A.
Koopmann, Tamara T.
Goyette, Philippe
Alikashani, Azadeh
Latour, Frédéric
Fatah, Meena
Hamilton, Robert M.
Rioux, John D.
author_facet Chaix, Marie-A.
Koopmann, Tamara T.
Goyette, Philippe
Alikashani, Azadeh
Latour, Frédéric
Fatah, Meena
Hamilton, Robert M.
Rioux, John D.
author_sort Chaix, Marie-A.
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spelling pubmed-54197572017-05-10 Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy Chaix, Marie-A. Koopmann, Tamara T. Goyette, Philippe Alikashani, Azadeh Latour, Frédéric Fatah, Meena Hamilton, Robert M. Rioux, John D. HeartRhythm Case Rep Case Report Elsevier 2016-03-16 /pmc/articles/PMC5419757/ /pubmed/28491681 http://dx.doi.org/10.1016/j.hrcr.2016.02.002 Text en © 2016 Heart Rhythm Society. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Chaix, Marie-A.
Koopmann, Tamara T.
Goyette, Philippe
Alikashani, Azadeh
Latour, Frédéric
Fatah, Meena
Hamilton, Robert M.
Rioux, John D.
Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy
title Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy
title_full Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy
title_fullStr Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy
title_full_unstemmed Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy
title_short Novel CALM3 mutations in pediatric long QT syndrome patients support a CALM3-specific calmodulinopathy
title_sort novel calm3 mutations in pediatric long qt syndrome patients support a calm3-specific calmodulinopathy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419757/
https://www.ncbi.nlm.nih.gov/pubmed/28491681
http://dx.doi.org/10.1016/j.hrcr.2016.02.002
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