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dc.contributor.authorTezcan, Ilhan
dc.contributor.authorCamcioglu, Yildiz
dc.contributor.authorYegin, Olcay
dc.contributor.authorSanal, Ozden
dc.contributor.authorRoos, Dirk
dc.contributor.authorKÖKER, MUSTAFA YAVUZ
dc.contributor.authorvan Leeuwen, Karin
dc.contributor.authorKILIÇ, SARA ŞEBNEM
dc.contributor.authorBarlan, Isil
dc.contributor.authorYILMAZ, MUSTAFA
dc.contributor.authorMetin, Ayse
dc.contributor.authorde Boer, Martin
dc.contributor.authorAVCILAR, HÜSEYİN
dc.contributor.authorPATIROĞLU, TÜRKAN
dc.contributor.authorYILDIRAN, ALİŞAN
dc.date.accessioned2021-03-03T10:25:48Z
dc.date.available2021-03-03T10:25:48Z
dc.date.issued2013
dc.identifier.citationKÖKER M. Y. , Camcioglu Y., van Leeuwen K., KILIÇ S. Ş. , Barlan I., YILMAZ M., Metin A., de Boer M., AVCILAR H., PATIROĞLU T., et al., "Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients", JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, cilt.132, sa.5, ss.1156-1168, 2013
dc.identifier.issn0091-6749
dc.identifier.othervv_1032021
dc.identifier.otherav_227a093b-9bf7-4b16-8cbb-a7d6dc293ee6
dc.identifier.urihttp://hdl.handle.net/20.500.12627/28198
dc.identifier.urihttps://doi.org/10.1016/j.jaci.2013.05.039
dc.description.abstractBackground: Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disorder of phagocytes resulting in impaired killing of bacteria and fungi. A mutation in one of the 4 genes encoding the components p22(phox), p47(phox), p67(phox), and p40(phox) of the leukocyte nicotinamide dinucleotide phosphate reduced (NADPH) oxidase leads to autosomal recessive (AR) CGD. A mutation in the CYBB gene encoding gp91(phox) leads to X-linked recessive CGD.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectİmmünoloji
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectALERJİ
dc.subjectYaşam Bilimleri
dc.titleClinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients
dc.typeMakale
dc.relation.journalJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
dc.contributor.departmentErciyes Üniversitesi , Tıp Fakültesi , İmmünoloji
dc.identifier.volume132
dc.identifier.issue5
dc.identifier.startpage1156
dc.identifier.endpage1168
dc.contributor.firstauthorID211714


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