Single nucleotide polymorphisms of the very low density lipoprotein receptor (VLDLR) gene

Journal of Human Genetics

Volumn 46, Issue 8, 2001, Pages 490-493

  Near, S E ^a   Wang, J ^a   Hegele, R A ^a  

^a ROBARTS RESEARCH INSTITUTE   (Canada)

Author keywords

Alzheimer's disease; Atherosclerosis; Complex traits; Genomic DNA; Lipoproteins; Metabolism; Sequencing

Indexed keywords

VERY LOW DENSITY LIPOPROTEIN RECEPTOR;

3' UNTRANSLATED REGION; ALLELE; ALZHEIMER DISEASE; ARTICLE; CONTROLLED STUDY; EXON; FAMILIAL HYPERLIPEMIA; GENE AMPLIFICATION; GENETIC ASSOCIATION; GENETIC LINKAGE; HUMAN; INTRON; LIPOPROTEIN METABOLISM; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

3' UNTRANSLATED REGIONS; ALLELES; ELECTROPHORESIS, POLYACRYLAMIDE GEL; EXONS; GENOTYPE; HUMANS; HYPERLIPIDEMIA, FAMILIAL COMBINED; INTRONS; LIPOPROTEINS, VLDL; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, LDL; VARIATION (GENETICS);

EID: 0034890792     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380170051     Document Type: Article

References (3)

1. Human very-low-density lipoprotein receptor complementary DNA and deduced amino acid sequence and localization of its gene (VLDLR) to chromosome band 9q24 by fluorescence in situ hybridization
2. Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease
3. Common and rare ABCA1 variants affecting plasma HDL cholesterol