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HAX-1 deficiency: Characteristics of five cases including an asymptomatic patient

dc.contributor.authorÖner, Ozlem
dc.contributor.authorKeskindemirci, Gonca
dc.contributor.authorAKINEL, Aysenur
dc.contributor.authorBornaun, Helen
dc.contributor.authorHocaoglu, Arzu Babayigit
dc.contributor.authorKutluk, Gunsel
dc.contributor.authorAydoğmuş, Cigdem
dc.contributor.authorÇipe, Funda
dc.contributor.authorTAS, Melda
dc.date.accessioned2021-03-04T11:23:58Z
dc.date.available2021-03-04T11:23:58Z
dc.date.issued2016
dc.identifier.citationAydoğmuş C., Çipe F., TAS M., AKINEL A., Öner O., Keskindemirci G., Bornaun H., Kutluk G., Hocaoglu A. B. , "HAX-1 deficiency: Characteristics of five cases including an asymptomatic patient", ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY, cilt.34, sa.1, ss.73-76, 2016
dc.identifier.issn0125-877X
dc.identifier.othervv_1032021
dc.identifier.otherav_722b8495-a087-4937-9c01-c22c6445aa8d
dc.identifier.urihttp://hdl.handle.net/20.500.12627/78585
dc.identifier.urihttps://doi.org/10.12932/ap0618.34.1.2016
dc.description.abstractBackground: Mutations in the HAX-1 gene cause an autosomal recessive form of severe congenital neutropenia (SCN), which particularly manifests with recurrent skin, lung and deep tissue infections from the first few months of life.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectYaşam Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectİmmünoloji
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectALERJİ
dc.titleHAX-1 deficiency: Characteristics of five cases including an asymptomatic patient
dc.typeMakale
dc.relation.journalASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY
dc.contributor.departmentIstanbul Kanuni Sultan Suleyman Training & Research Hospital , ,
dc.identifier.volume34
dc.identifier.issue1
dc.identifier.startpage73
dc.identifier.endpage76
dc.contributor.firstauthorID104373


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