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

Internet

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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