Mutational and genetic origin of LDL receptor gene mutations detected in both Belgian and Dutch familial hypercholesterolemics

Human Genetics

Volumn 100, Issue 2, 1997, Pages 266-270

  Peeters, A V ^a   Van Gaal, L F ^a   Du Plessis, L ^a   Lombardi, M P R ^a   Havekes, L M ^a   Kotze, M J ^a  

^a UNIVERSITY OF STELLENBOSCH   (South Africa)

Author keywords

[No Author keywords available]

Indexed keywords

LOW DENSITY LIPOPROTEIN RECEPTOR;

ARTICLE; BELGIUM; COMPARATIVE STUDY; CONTROLLED STUDY; EXON; FAMILIAL HYPERCHOLESTEROLEMIA; GENE DELETION; GENE MUTATION; GENE REARRANGEMENT; GENE SEQUENCE; HAPLOTYPE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; NETHERLANDS; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RECEPTOR GENE; SOUTHERN BLOTTING;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; BASE SEQUENCE; BELGIUM; CLONING, MOLECULAR; FEMALE; GENETIC SCREENING; HAPLOTYPES; HUMANS; HYPERLIPOPROTEINEMIA TYPE II; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; NETHERLANDS; POLYMERASE CHAIN REACTION; RECEPTORS, LDL; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION;

EID: 0030791322     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050503     Document Type: Article

References (26)