Heterozygous familial hypercholesterolemia (FH) is a relatively common autosomal dominant disorder, which is characterized by elevated plasma concentrations of low density lipoprotein (LDL) cholesterol and early coronary heart disease. FH results from mutations in the gene encoding the LDL receptor
Identification of three mutations in the low-density lipoprotein receptor gene causing familial hypercholesterolemia among French Canadians
✍ Scribed by Patrick Couture; Marie-Claude Vohl; Claude Gagné; Daniel Gaudet; Ana L. Torres; Paul J. Lupien; Jean-Pierre Després; Fernand Labrie; Dr. Jacques Simard; Sital Moorjani
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 751 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1059-7794
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