Elevated blood plasma cholesterol (hypercholesterolemia) is a major risk factor for coronary artery disease (CAD) in humans. Genetic dissection of polygenic lipid and lipoprotein disorders in swine, a key animal model for the study of familial hypercholesterolemia (FH) and CAD, led to the isolation
Identification of a mutation, N543H, in exon 11 of the low-density lipoprotein receptor gene in a French family with familial hypercholesterolemia
โ Scribed by F. Tricot-Guerber; B. Saint-Jore; K. Valenti; T. Foulon; M. Bost; A. J. Hadjian
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 183 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1059-7794
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Familial hypercholesterolemia (FH) is a common autosomal dominant disorder of lipid metabolism caused by mutations