Proprotein convertase subtilisin/kexin 9 V4I variant with LDLR mutations modifies the phenotype of familial hypercholesterolemia

Published 2016 View Full Article

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Title
Proprotein convertase subtilisin/kexin 9 V4I variant with LDLR mutations modifies the phenotype of familial hypercholesterolemia
Authors
Keywords
PCSK9, LDL receptor, Variant, Familial hypercholesterolemia, Mutation
Journal
Journal of Clinical Lipidology
Volume 10, Issue 3, Pages 547-555.e5
Publisher
Elsevier BV
Online
2016-01-07
DOI
10.1016/j.jacl.2015.12.024

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