Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology

Marzia De Bortoli, Riccardo Vio, Cristina Basso, Martina Calore, Giovanni Minervini, Annalisa Angelini, Paola Melacini, Libero Vitiello, Giovanni Vazza, Gaetano Thiene, Silvio Tosatto, Domenico Corrado, Sabino Iliceto, Alessandra Rampazzo*, Chiara Calore

*Corresponding author for this work

Research output: Contribution to journalComment/Letter to the editorAcademicpeer-review

Original languageEnglish
Article number002824
Number of pages3
JournalCirculation: Genomic and Precision Medicine
Volume13
Issue number4
DOIs
Publication statusPublished - Apr 2020

Keywords

  • atrial fibrillation
  • cardiomyopathies
  • disease
  • genes
  • prognosis

Cite this

De Bortoli, M., Vio, R., Basso, C., Calore, M., Minervini, G., Angelini, A., Melacini, P., Vitiello, L., Vazza, G., Thiene, G., Tosatto, S., Corrado, D., Iliceto, S., Rampazzo, A., & Calore, C. (2020). Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology. Circulation: Genomic and Precision Medicine, 13(4), [002824]. https://doi.org/10.1161/CIRCGEN.119.002824