Genetic analysis of Iranian patients with familial hypercholesterolemia
IBJ-Iranian Biomedical Journal. 2018; 22 (2): 117-122
en Inglés
| IMEMR
| ID: emr-192458
ABSTRACT
Background:
Familial hypercholesterolemia [FH] is a frequent autosomal dominant disorder of lipoprotein metabolism. This disorder is generally caused by mutations in low-density lipoprotein receptor [LDLR], apolipoprotein B 100 [APOB], and proprotein convertase subtilisin/kexin type 9 [PCSK9] genes. In the present study, we aimed at identifying the common LDLR and APOB gene mutations in an Iranian population
Buscar en Google
Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Receptores de LDL
/
Apolipoproteína B-100
/
Genética
Límite:
Adulto
/
Anciano
/
Femenino
/
Humanos
/
Masculino
Idioma:
Inglés
Revista:
Iran. Biomed. J.
Año:
2018
Similares
MEDLINE
...
LILACS
LIS