Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology.
Circ Genom Precis Med
; 13(2): e002824, 2020 04.
Article
in En
| MEDLINE
| ID: mdl-32004434
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Atrial Fibrillation
/
Cardiomyopathy, Hypertrophic
/
Myosin Light Chains
/
Mutation, Missense
/
Cardiac Myosins
Type of study:
Incidence_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Adult
/
Aged
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
/
Middle aged
Country/Region as subject:
Europa
Language:
En
Journal:
Circ Genom Precis Med
Year:
2020
Type:
Article
Affiliation country:
Italy