FH clinical phenotype in Greek patients with LDL-R defective vs. negative mutations
Author:
Publisher
Wiley
Subject
Clinical Biochemistry,Biochemistry,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2362.2004.01351.x/fullpdf
Reference31 articles.
1. Low-density lipoprotein receptor gene (LDLR) world-wide website in familial hypercholesterolaemia: update, new features and mutation analysis
2. LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis
3. Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.
4. Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100.
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