An Avall polymorphism in the human apolipoprotein C-II gene

Clinical Genetics

Volumn 49, Issue 3, 1996, Pages 163-

  Geisel, J ^a   Weisshaar C ^a   Oette, K ^a  

^a UNIVERSITY OF COLOGNE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEIN C2; DNA MARKER;

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 19Q; GENE FREQUENCY; HETEROZYGOSITY; HUMAN; INHERITANCE; NORMAL HUMAN; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

APOLIPOPROTEIN C-II; APOLIPOPROTEINS C; BASE SEQUENCE; BINDING SITES; CHROMOSOMES, HUMAN, PAIR 19; DEOXYRIBONUCLEASES, TYPE II SITE-SPECIFIC; EUROPEAN CONTINENTAL ANCESTRY GROUP; GENE FREQUENCY; GENETIC MARKERS; HETEROZYGOTE; HUMANS; HYPERLIPOPROTEINEMIA TYPE I; MOLECULAR SEQUENCE DATA; PEDIGREE; POLYMORPHISM, GENETIC;

EID: 0030060923     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb03278.x     Document Type: Article

References (2)

1. Das HK, Jackson CL, Miller DA, Leff T, Breslow JL. The human apolipoprotein C-II gene sequence contains a novel chromosome 19-specific minisatellite in its third intron. J Biol Chem 1987: 262: 4787-4793.
2. Korneluk RG, MacLeod HL, Leblond SC, Monteith NL, Baralle FE, Hunter AGW. AvaII RFLP at the human apolipoprotein CII (apo CII) gene locus. Nucl Acids Res 1987: 15: 6769.