Allele-specific and asymmetric polymerase chain reaction amplification in combination: A one step polymerase chain reaction protocol for rapid diagnosis of familial defective apolipoprotein B-100
- 1 July 1992
- journal article
- Published by Elsevier in Analytical Biochemistry
- Vol. 204 (1) , 22-25
- https://doi.org/10.1016/0003-2697(92)90133-r
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Familial defective apolipoprotein B-100: Haplotype analysis of the arginine(3500) → glutamine mutationAtherosclerosis, 1991
- Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplificationThe Lancet, 1990
- Familial defective apolipoprotein B-100. Comparison with familial hypercholesterolemia in 18 cases detected in Munich.Arteriosclerosis: An Official Journal of the American Heart Association, Inc., 1990
- Two common low density lipoprotein receptor gene mutations cause familial hypercholesterolemia in Afrikaners.Journal of Clinical Investigation, 1989
- Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markersNucleic Acids Research, 1989
- Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probesNature, 1986