MS70 STUDY ON THE MOLECULAR BASIS OF FAMILIAL HYPERCHOLESTEROLEMIA IN MEXICO. ADVANCES OF PROJECT
✍ Scribed by Vaca, G.; Vázquez, A.; Magaña, M.T.; Ramírez, M.L.; Dávalos, I.P.; Marín, B.; Martínez, E.; Carrillo, G.
- Book ID
- 118638576
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 55 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1567-5688
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Autosomal-dominant hypercholesterolemia (ADH) has been identified as a major risk factor for coronary vascular disease (CVD) and is associated with mutations in the low-density lipoprotein receptor (LDLR) and the apolipoprotein B (APOB) gene. Since 1991 DNA samples from clinically diagnosed ADH pati
Autosomal dominant hypercholesterolemia (ADH), a major risk for coronary heart disease, is associated with mutations in the genes encoding the low-density lipoproteins receptor (LDLR), its ligand apolipoprotein B (APOB) or PCSK9 (Proprotein Convertase Subtilin Kexin 9). Familial hypercholesterolemia