Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemia
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2006.00585.x/fullpdf
Reference40 articles.
1. The LDL receptor locus in familial hypercholesterolemia: mutational analysis of a membrane protein;Hobbs;Annu Rev Genet,1990
2. Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemia;Thiart;J Med Genet,2000
3. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia;Hobbs;Hum Mutat,1992
4. Spectrum of LDL-receptor gene mutations in heterozygous familial hypercholesterolemia;Day;Hum Mutat,1997
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