The c.43_44insCTG variation inPCSK9 is associated with low plasma LDL-cholesterol in a Caucasian population
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference34 articles.
1. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
2. Novel mutations of thePCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia
3. High-Density Lipoprotein Function
4. NARC-1/PCSK9 and Its Natural Mutants
5. A Novel Nontruncating APOB Gene Mutation, R463W, Causes Familial Hypobetalipoproteinemia
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