PCSK9: an emerging target for treatment of hypercholesterolemia
Author:
Publisher
Informa Healthcare
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1517/14728222.2011.547480
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2. Familial defective apolipoprotein B-100: low density lipoproteins with abnormal receptor binding.
3. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
4. A Third Major Locus for Autosomal Dominant Hypercholesterolemia Maps to 1p34.1-p32
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