Publication:
A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency

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dc.contributor.authorÖZEN, AHMET OĞUZHAN
dc.contributor.authorAYDINER, ELİF
dc.contributor.authorBARIŞ, SAFA
dc.contributor.authorsFirtina, Sinem; Cipe, Funda; Ng, Yuk Yin; Kiykim, Ayca; Ng, Ozden Hatirnaz; Sudutan, Tugce; Aydogmus, Cigdem; Baris, Safa; Ozturk, Gulyuz; Aydiner, Elif; Ozen, Ahmet; Sayitoglu, Muge
dc.date.accessioned2022-03-15T12:01:10Z
dc.date.accessioned2026-01-11T08:02:14Z
dc.date.available2022-03-15T12:01:10Z
dc.date.issued2019
dc.identifier.doi10.1007/s10875-019-00615-6
dc.identifier.issn1573-2592
dc.identifier.pubmedPMID: 30903456
dc.identifier.urihttps://hdl.handle.net/11424/252894
dc.language.isoeng
dc.relation.ispartofJournal of Clinical Immunology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectFemale
dc.subjectHumans
dc.subjectTurkey
dc.subjectInfant
dc.subjectMale
dc.subjectConsanguinity
dc.subjectForkhead Transcription Factors
dc.subjectSiblings
dc.subjectSevere Combined Immunodeficiency
dc.titleA Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage147
oaire.citation.startPage144
oaire.citation.titleJournal of Clinical Immunology
oaire.citation.volume2

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