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

Authors :: Paola Melacini
Martina Calore
Giovanni Minervini
Libero Vitiello
Annalisa Angelini
Silvio C. E. Tosatto
Giovanni Vazza
Riccardo Vio
Cristina Basso
Gaetano Thiene
Alessandra Rampazzo
Sabino Iliceto
Chiara Calore
Marzia De Bortoli
Domenico Corrado
Cardiologie
RS: FSE DMG
RS: Carim - H05 Gene regulation
Source :: Circulation: Genomic and Precision Medicine, 13(2):002824. Lippincott Williams and Wilkins Ltd.
Publication Year :: 2020
Publisher :: Ovid Technologies (Wolters Kluwer Health), 2020.

Subjects :: cardiomyopathies
disease
business.industry
Hypertrophic cardiomyopathy
Atrial fibrillation
General Medicine
Disease
Bioinformatics
medicine.disease
atrial fibrillation
genes
prognosis
MYL2
Missense mutation
Medicine
High incidence
business
Gene

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