Low frequency of the common Norwegian and Finnish LDL‐receptor mutations in Swedish patients with familial hypercholesterolaemia - Lind, S.; Eriksson, M.; Rystedt, E.; Wiklund, O.; Angelin, B.; Eggertsen, G. (Journal of internal medicine, 1998)
Keywords: Adult; Aged; atherosclerosis; Biological and medical sciences; Disorders of blood lipids. Hyperlipoproteinemia; Exons - genetics; familial hypercholesterolaemia; Female; Finland; Gene Frequency; Humans; Hyperlipoproteinemia Type II - genetics; low‐density lipoprotein receptor; Male; Medical sciences; Metabolic diseases; Middle Aged; Mutation; mutations; Norway; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Receptors, LDL - genetics; Sweden; Sweden; Europe; Norway; Finland; Human; Metabolic diseases; Exploration; Lipids; Hyperlipoproteinemia; Genetic disease; Lipoprotein LDL; Hypercholesterolemia; Gene; Genetics; Frequency; Mutation; Dyslipemia; Biological receptor