The Trp23-Stop and Trp66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark.

Jensen, H K; Jensen, L G; Hansen, P S; Faergeman, O; Gregersen, N

Jensen, H K; Jensen, L G; Hansen, P S; Faergeman, O; Gregersen, N.

Affiliation

Jensen HK; Center for Medical Molecular Biology, Skejby Sygehus University Hospital, Arhus N, Denmark.

Atherosclerosis ; 120(1-2): 57-65, 1996 Feb.

Article in En | MEDLINE | ID: mdl-8645371

Subject(s)

Hyperlipoproteinemia Type II/genetics; Point Mutation; Receptors, LDL/genetics; Adult; Aged; Base Sequence; Canada/epidemiology; Cholesterol/blood; Cholesterol, HDL/blood; Cholesterol, LDL/blood; Codon/genetics; DNA Mutational Analysis; Denmark/epidemiology; Female; France/ethnology; Gene Frequency; Genes; Haplotypes/genetics; Humans; Hyperlipoproteinemia Type II/blood; Hyperlipoproteinemia Type II/epidemiology; Male; Middle Aged; Molecular Sequence Data; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Prevalence; Triglycerides/blood

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Database: MEDLINE Main subject: Receptors, LDL / Point Mutation / Hyperlipoproteinemia Type II Type of study: Etiology_studies / Prevalence_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: America do norte / Europa Language: En Journal: Atherosclerosis Year: 1996 Type: Article Affiliation country: Denmark

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