Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia.
Sci Rep
; 7(1): 17921, 2017 12 20.
Article
in En
| MEDLINE
| ID: mdl-29263402
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Coronary Artery Disease
/
Ethnicity
/
Mutation, Missense
/
Polymorphism, Single Nucleotide
/
Genome-Wide Association Study
/
Apolipoprotein A-V
Type of study:
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Adult
/
Aged
/
Aged80
/
Female
/
Humans
/
Male
/
Middle aged
Country/Region as subject:
Asia
Language:
En
Journal:
Sci Rep
Year:
2017
Document type:
Article
Affiliation country:
Singapur
Country of publication:
Reino Unido