Phenotypical features of heterozygous familial hypercholesterolemia in individuals with LDLR or APOB gene mutations
Familial hypercholesterolemia (FHCH) is a hereditary autosomal dominant disease, characterised by lipid metabolism disturbances and high plasma levels of low-density lipoprotein cholesterol (LDL–CH). Aim. To compare lipid metabolism parameters in patients with various genetic variants of FHCH, and t...
Saved in:
| Main Authors: | , , , , , , |
|---|---|
| Format: | Article |
| Language: | Russian |
| Published: |
«SILICEA-POLIGRAF» LLC
1970-01-01
|
| Series: | Кардиоваскулярная терапия и профилактика |
| Subjects: | |
| Online Access: | https://cardiovascular.elpub.ru/jour/article/view/2065 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|