The Gln-Arg191 polymorphism of the human paraoxonase gene (HUMPONA) is not associated with the risk of coronary artery disease in Finns.

The human paraoxonase gene (HUMPONA) is codominantly expressed as alleles A and G. The A allele codes for glutamine (A genotype) and the G allele for arginine (B genotype) at position 191 of the paraoxonase enzyme. This genetic polymorphism has been suggested to be associated with the predisposition...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Antikainen, M, Murtomäki, S, Syvänne, M, Pahlman, R, Tahvanainen, E, Jauhiainen, M, Frick, M H, Ehnholm, C
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1996
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC507500/
https://ncbi.nlm.nih.gov/pubmed/8770857
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