Update and Analysis of the University College London Low Density Lipoprotein Receptor Familial Hypercholesterolemia Database
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-1809.2008.00436.x/fullpdf
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1. Intronic mutations outside of Alu -repeat-rich domains of the LDL receptor gene are a cause of familial hypercholesterolemia
2. Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemia
3. Identification of recurrent and novel mutations in the LDL receptor gene in Spanish patients with familial hypercholesterolemia
4. Identification and characterization of LDL receptor gene mutations in hyperlipidemic Chinese
5. Sequence Variations inPCSK9,Low LDL, and Protection against Coronary Heart Disease
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