Yayın:
MBL2 gene polymorphism and risk of vitiligo in Turkish patients

dc.contributor.authorKarkucak, Mutlu
dc.contributor.authorSolak, Berna
dc.contributor.authorTuran, Hakan
dc.contributor.authorUslu, Esma
dc.contributor.authorYakut, Tahsin
dc.contributor.authorAliagaoglu, Cihangir
dc.contributor.authorErdem, Teoman
dc.contributor.buuauthorYakut, Tahsin
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıbbi Genetik Ana Bilim Dalı
dc.contributor.orcid0000-0002-8661-6126
dc.contributor.scopusid6602802424
dc.date.accessioned2025-05-13T10:01:47Z
dc.date.issued2015-09-01
dc.description.abstractMannose-Binding Lectin (MBL) plays an important role in innate immunity. MBL2 gene polymorphisms affect MBL serum levels. Therefore, this increases the risk of infection and may result in predisposition to autoimmune diseases. The aim of this study was to investigate whether there is an association between the MBL2 gene codon 54 (allele B: rs1800450, c.161G>A; p.54Gly>Asp) polymorphism and vitiligo in Turkish patients. One hundred and one patients who were diagnosed with vitiligo and 101 control subjects were included in the study. The DNA was analyzed using the Kbioscience Competitive Allele Specific PCR (KASP) technique. MBL2 gene codon 54 polymorphism frequencies were compared between the two groups. In statistical analysis, the level of significance was set at p<0.05. No significant differences in frequencies of the A allele were observed between the patient and control groups. It was observed at similar frequencies in both groups (p=0.890). The results suggest that the MBL2 gene Codon 54 polymorphism is not associated with an increased risk for the development of vitiligo in Turkish patients.
dc.description.sponsorshipSakarya Üniversitesi - 2014-08-06-009
dc.identifier.doi10.1080/09723757.2015.11886257
dc.identifier.endpage96
dc.identifier.issn0972-3757
dc.identifier.issue3
dc.identifier.scopus2-s2.0-84942429790
dc.identifier.startpage93
dc.identifier.urihttps://hdl.handle.net/11452/52402
dc.identifier.volume15
dc.indexed.scopusScopus
dc.language.isoen
dc.publisherKamla-Raj Enterprises
dc.relation.journalInternational Journal of Human Genetics
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectVitiligo
dc.subjectPolymorphism
dc.subjectMannose-binding lectin
dc.subject.scopusVitiligo: Understanding Melanocyte Loss and Treatment
dc.titleMBL2 gene polymorphism and risk of vitiligo in Turkish patients
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Tıbbi Genetik Ana Bilim Dalı
local.indexed.atScopus

Dosyalar