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PMID: 8835321 Published · ppublish English Journal Article

Association between a dimorphic site on chromosome 12 and clinical diagnosis of hypertension in three independent populations.

Clinical genetics ·Vol. 48 ·No. 6 ·1995-12-00 ·Pages 284-7

Frossard PM, Lestringant GG

Abstract

With the aim of identifying putative quantitative trait loci (QTLs) involved in the regulation of blood pressure, we have carried out association studies at a candidate genetic locus-a human pancreatic phospholipase A2 (PLA2) gene localized on chromosome 12. Positive associations were found between the presence of a Taq I dimorphic site localized in the first intron of this gene and hypertension in three sample populations (two from USA and one from Germany). These results indicate that a QTL implicated in determining an individual's genetic susceptibility to hypertension could be present within up to 30 cM of this human PLA2 gene.

MeSH Terms
Chromosomes, Human, Pair 12 Deoxyribonucleases, Type II Site-Specific/metabolism Gene Frequency Humans Hypertension/genetics Leukocytes/physiology Middle Aged Pancreas/chemistry Phospholipases A/genetics Phospholipases A2 Polymorphism, Restriction Fragment Length Population Surveillance
Chemicals
Phospholipases A Phospholipases A2 Deoxyribonucleases, Type II Site-Specific TCGA-specific type II deoxyribonucleases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Frossard P M
Department of Pathology, Faculty of Medicine and Health Sciences, Al Ain, United Arab Emirates.
Lestringant G G
Article Info
Journal
Clinical genetics
Abbr.
Clin Genet
ISSN
0009-9163
Published
1995-12-00
Pages
284-7
Language
English
Region
Denmark
NLM ID
0253664
Subset
IM
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