Dual myosin binding protein C3 and potassium voltage-gated channel subfamily H member 2 co-inherited pathogenic variants in a patient with hypertrophic cardiomyopathy and long QT 2 syndrome: A case report

Detalles Bibliográficos
Autores principales: Alvarez, Chikezie K., Smith, Emily, Weissler-Snir, Adaya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039531/
https://www.ncbi.nlm.nih.gov/pubmed/35492841
http://dx.doi.org/10.1016/j.hrcr.2021.12.010
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author Alvarez, Chikezie K.
Smith, Emily
Weissler-Snir, Adaya
author_facet Alvarez, Chikezie K.
Smith, Emily
Weissler-Snir, Adaya
author_sort Alvarez, Chikezie K.
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spelling pubmed-90395312022-04-27 Dual myosin binding protein C3 and potassium voltage-gated channel subfamily H member 2 co-inherited pathogenic variants in a patient with hypertrophic cardiomyopathy and long QT 2 syndrome: A case report Alvarez, Chikezie K. Smith, Emily Weissler-Snir, Adaya HeartRhythm Case Rep Case Report Elsevier 2021-12-16 /pmc/articles/PMC9039531/ /pubmed/35492841 http://dx.doi.org/10.1016/j.hrcr.2021.12.010 Text en © 2021 Heart Rhythm Society. Published by Elsevier Inc. https://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
Alvarez, Chikezie K.
Smith, Emily
Weissler-Snir, Adaya
Dual myosin binding protein C3 and potassium voltage-gated channel subfamily H member 2 co-inherited pathogenic variants in a patient with hypertrophic cardiomyopathy and long QT 2 syndrome: A case report
title Dual myosin binding protein C3 and potassium voltage-gated channel subfamily H member 2 co-inherited pathogenic variants in a patient with hypertrophic cardiomyopathy and long QT 2 syndrome: A case report
title_full Dual myosin binding protein C3 and potassium voltage-gated channel subfamily H member 2 co-inherited pathogenic variants in a patient with hypertrophic cardiomyopathy and long QT 2 syndrome: A case report
title_fullStr Dual myosin binding protein C3 and potassium voltage-gated channel subfamily H member 2 co-inherited pathogenic variants in a patient with hypertrophic cardiomyopathy and long QT 2 syndrome: A case report
title_full_unstemmed Dual myosin binding protein C3 and potassium voltage-gated channel subfamily H member 2 co-inherited pathogenic variants in a patient with hypertrophic cardiomyopathy and long QT 2 syndrome: A case report
title_short Dual myosin binding protein C3 and potassium voltage-gated channel subfamily H member 2 co-inherited pathogenic variants in a patient with hypertrophic cardiomyopathy and long QT 2 syndrome: A case report
title_sort dual myosin binding protein c3 and potassium voltage-gated channel subfamily h member 2 co-inherited pathogenic variants in a patient with hypertrophic cardiomyopathy and long qt 2 syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039531/
https://www.ncbi.nlm.nih.gov/pubmed/35492841
http://dx.doi.org/10.1016/j.hrcr.2021.12.010
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