Rare and Deleterious Mutations in ABCG5/ABCG8 Genes Contribute to Mimicking and Worsening of Familial Hypercholesterolemia Phenotype.
Circ J
; 83(9): 1917-1924, 2019 08 23.
Article
in En
| MEDLINE
| ID: mdl-31327807
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Cholesterol
/
ATP Binding Cassette Transporter, Subfamily G, Member 5
/
ATP Binding Cassette Transporter, Subfamily G, Member 8
/
Hyperlipoproteinemia Type II
/
Lipoproteins
/
Mutation
Type of study:
Diagnostic_studies
/
Etiology_studies
/
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Adult
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Circ J
Journal subject:
ANGIOLOGIA
/
CARDIOLOGIA
Year:
2019
Type:
Article