The molecular basis of familial hypercholesterolemia in the Netherlands

Human Genetics

Volumn 109, Issue 6, 2001, Pages 602-615

  Fouchier, Sigrid W ^a,b   Defesche, Joep C ^a,b   Umans Eckenhausen, Marina A ^a,b   Kastelein, John J ^a,b  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

^b Foundation for the Identification of Persons with Inherited Hypercholesterolemia   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

LOW DENSITY LIPOPROTEIN RECEPTOR;

AMINO ACID SEQUENCE; ARTICLE; CARDIOVASCULAR DISEASE; CLINICAL TRIAL; COHORT ANALYSIS; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; DISEASE CLASSIFICATION; FAMILIAL HYPERCHOLESTEROLEMIA; FAMILIAL INCIDENCE; GEL ELECTROPHORESIS; GENE MUTATION; GENE SEQUENCE; GENETIC DISORDER; GENETIC SCREENING; HEALTH PROGRAM; HIGH RISK PATIENT; HUMAN; MOLECULAR GENETICS; MORBIDITY; MORTALITY; MUTATIONAL ANALYSIS; NETHERLANDS; PATIENT SELECTION; POPULATION GENETICS; PRIORITY JOURNAL;

GENE FREQUENCY; GENETIC SCREENING; HUMANS; HYPERLIPOPROTEINEMIA TYPE II; MUTATION; NETHERLANDS; RECEPTORS, LDL;

EID: 0035686835     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-001-0628-8     Document Type: Article

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