A Novel Splicing Variant of Proprotein Convertase Subtilisin/Kexin Type 9
Author:
Affiliation:
1. Lilly Research Laboratories, Eli Lilly & Company, Indianapolis, Indiana.
Publisher
Mary Ann Liebert Inc
Subject
Cell Biology,Genetics,Molecular Biology,General Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/dna.2007.0667
Reference23 articles.
1. Mutations in PCSK9 cause autosomal dominant hypercholesterolemia
2. NARC-1/PCSK9 and Its Natural Mutants
3. Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9
4. Sequence Variations inPCSK9,Low LDL, and Protection against Coronary Heart Disease
5. Structural and biophysical studies of PCSK9 and its mutants linked to familial hypercholesterolemia
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