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IMPACT OF LOW-DENSITY LIPOPROTEIN RECEPTOR (LDLR) MUTATIONAL CLASS ON CAROTID ATHEROSCLEROSIS IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA (FH)

✍ Scribed by Junyent, M.; Gilabert, R.; Nunez, I.; Pocovi, M.; Mallen, M.; Zambon, D.; Jarauta, E.; Civeira, F.; Vega, J.; Almagro, F.; Ros, E.

Book ID: 118636295
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 86 KB
Volume: 9
Category: Article
ISSN: 1567-5688
DOI: 10.1016/s1567-5688(08)70452-5

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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