Diagnosis of familial hypercholesterolemia in general practice using clinical diagnostic criteria or genetic testing as part of cascade genetic screening

Community Genetics

Volumn 11, Issue 1, 2008, Pages 26-35

  Leren, Trond P ^a   Finborud, Tora Himle ^b   Manshaus, Turid E ^a   Ose, Leiv ^a   Berge, Knut Erik ^a  

^a OSLO UNIVERSITY HOSPITAL   (Norway)

^b NORWEGIAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Norway)

Author keywords

Familial hypercholesterolemia; Genetics; Lipoproteins; Mutation; Prevention; Screening

Indexed keywords

ANTILIPEMIC AGENT; LOW DENSITY LIPOPROTEIN CHOLESTEROL;

ADULT; ARTICLE; CHOLESTEROL BLOOD LEVEL; CONTROLLED STUDY; FAMILIAL HYPERCHOLESTEROLEMIA; FEMALE; FOLLOW UP; GENE MUTATION; GENERAL PRACTICE; GENETIC SCREENING; GOLD STANDARD; HUMAN; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; PRIORITY JOURNAL; QUESTIONNAIRE; SENSITIVITY AND SPECIFICITY;

ADULT; DNA MUTATIONAL ANALYSIS; EXONS; FAMILY HEALTH; FEMALE; FOLLOW-UP STUDIES; GENETIC SCREENING; HUMANS; HYPERLIPOPROTEINEMIA TYPE II; MALE; MIDDLE AGED; MUTATION; NORWAY; TIME FACTORS;

EID: 38349058652     PISSN: 14222795     EISSN: None     Source Type: Journal    
DOI: 10.1159/000111637     Document Type: Article

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