Show simple item record

THE ROLE OF 21-HYDROXYLASE DEFICIENCY IN THE PATHOGENESIS OF BEHCET DISEASE

dc.contributor.authorAral, Orhan
dc.contributor.authorGul, Nurdan
dc.contributor.authorAlagol, Faruk
dc.contributor.authorInanc, Murat
dc.contributor.authorOcal, Lale
dc.contributor.authorGül, Ahmet
dc.date.accessioned2021-03-04T10:09:28Z
dc.date.available2021-03-04T10:09:28Z
dc.date.issued2018
dc.identifier.citationGul N., Gül A., Inanc M., Ocal L., Aral O., Alagol F., "THE ROLE OF 21-HYDROXYLASE DEFICIENCY IN THE PATHOGENESIS OF BEHCET DISEASE", JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI, cilt.81, sa.1, ss.11-16, 2018
dc.identifier.othervv_1032021
dc.identifier.otherav_6bc18dd8-b1bd-491a-80ec-0bfb90b1cb0b
dc.identifier.urihttp://hdl.handle.net/20.500.12627/74502
dc.description.abstractObjective: Acne-like skin lesions and more severe disease course in males suggest a role for sex hormones in the pathogenesis of Behcet disease (BD). HLA-B51 is the main genetic susceptibility factor for BD, and CYP21A2 gene responsible for most of congenital adrenal hyperplasia (CAH) is located within the MHC locus on chromosome 6p21.3. We aimed to investigate the possible role of 21-hydroxylase deficiency in linkage disequilibrium with HLA-B51 and causing androgen excess.
dc.language.isoeng
dc.subjectTıp
dc.subjectTemel Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleTHE ROLE OF 21-HYDROXYLASE DEFICIENCY IN THE PATHOGENESIS OF BEHCET DISEASE
dc.typeMakale
dc.relation.journalJOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
dc.contributor.departmentİstanbul Teknik Üniversitesi , Fen-Edebiyat , Kimya
dc.identifier.volume81
dc.identifier.issue1
dc.identifier.startpage11
dc.identifier.endpage16
dc.contributor.firstauthorID102311


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record