Mutations in the low-density-lipoprotein receptor gene in German patients with familial hypercholesterolaemia
Author:
Affiliation:
1. ; Medizinische Poliklinik; University of Munich; Germany
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1026704517598/fullpdf
Reference39 articles.
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2. Four novel partial deletions of LDL-receptor gene in Italian patients with familial hypercholesterolemia;Bertolini;Arterioscler Thromb Vasc Biol,1995
3. Influuence of genetic variability in the nondeletion LDL-receptor allele on phenotypic variation in French-Canadian familial hypercholesterolemia heterozygotes sharing a ‘null’ LDL-receptor gene defect;Betard;Atherosclerosis,1996
4. Plasma level and gene polymorphism of angiotensin-converting enzyme in relation to myocardial infarction;Cambien;Circulation,1994
5. Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia;Day;Hum Mutat,1997
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