Paroxonase (PON1-L55M) gene polymorphism and its association with Behçet's disease among Iranian population

Ophthalmic Genet. 2020 Jun;41(3):293-294. doi: 10.1080/13816810.2020.1747087. Epub 2020 Apr 24.

Authors

Samaneh Mesgari¹, Saba A Nazm², Mortaza Bonyadi², Mohammad Hossein Jabbarpoor Bonyadi³, Masoud Soheilian³

Affiliations

¹ Department of Biology, School of Genetic, Azad University of Tabriz , Tabriz, Iran.
² Center of Excellence for Biodiversity, Faculty of Natural Sciences, University of Tabriz , Tabriz, Iran.
³ Ocular Tissue Engineering Research Center, Ophthalmic Research Center, Shahid Beheshti Universith of Medical Sciences , Tehran, Iran.

PMID: 32326787
DOI: 10.1080/13816810.2020.1747087

No abstract available

MeSH terms

Aryldialkylphosphatase / genetics*
Behcet Syndrome / epidemiology*
Behcet Syndrome / genetics
Behcet Syndrome / pathology
Case-Control Studies
Genetic Predisposition to Disease*
Genotype
Humans
Iran / epidemiology
Polymorphism, Single Nucleotide*

Substances

Aryldialkylphosphatase
PON1 protein, human