Identification of recurrent and novel mutations in the LDL receptor gene in German patients with familial hypercholesterolemia

Human mutation

Volumn 18, Issue 2, 2001, Pages 165-166

  Nauck, M S ^a   Koster W ^a   Dorfer K ^a   Eckes, J ^a   Scharnagl, H ^a   Gierens, H ^a   Nissen, H ^b   Nauck, M A ^a   Wieland, H ^a   März, Winfried ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

^b ODENSE UNIVERSITY HOSPITAL   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN B; APOLIPOPROTEIN B100; LOW DENSITY LIPOPROTEIN RECEPTOR;

ADOLESCENT; ADULT; AGED; ARTICLE; BLOOD; CHILD; CODON; COHORT ANALYSIS; CPG ISLAND; EXON; FEMALE; GENE FREQUENCY; GENETIC SCREENING; GENETICS; GERMANY; HUMAN; HYPERLIPOPROTEINEMIA TYPE 2; INTRON; MALE; MIDDLE AGED; MUTATION; NUCLEOTIDE SEQUENCE; PROMOTER REGION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ADOLESCENT; ADULT; AGED; APOLIPOPROTEIN B-100; APOLIPOPROTEINS B; CHILD; CODON; COHORT STUDIES; CPG ISLANDS; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENE FREQUENCY; GENETIC SCREENING; GERMANY; HUMANS; HYPERLIPOPROTEINEMIA TYPE II; INTRONS; MALE; MIDDLE AGED; MUTATION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PROMOTER REGIONS (GENETICS); RECEPTORS, LDL;

EID: 0035433386     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.1171     Document Type: Article

References (0)