Publication:
A novel homozygous frameshift CCNO variant presenting with primary ciliary dyskinesia and selective IGM deficiency

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dc.contributor.coauthorCeliksoy, Mehmet Halil
dc.contributor.coauthorTuran, Isilay
dc.contributor.coauthorGezdirici, Alper
dc.contributor.coauthorAydogmus, Cigdem
dc.contributor.coauthorNaiboglu, Sezin
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.kuauthorKayalar, Özgecan
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2025-01-19T10:32:22Z
dc.date.issued2023
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue11
dc.description.openaccessBronze
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.volume58
dc.identifier.doi10.1002/ppul.26607
dc.identifier.eissn1099-0496
dc.identifier.issn8755-6863
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85165970917
dc.identifier.urihttps://doi.org/10.1002/ppul.26607
dc.identifier.urihttps://hdl.handle.net/20.500.14288/26392
dc.identifier.wos1037685700001
dc.keywordsBronchiectasis
dc.keywordsCCNO gene
dc.keywordsPrimary immunodeficiency
dc.keywordsPrimary siliary dyskinesia
dc.keywordsSelective IgM deficiency
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofPediatric Pulmonology
dc.subjectPediatrics
dc.subjectRespiratory system
dc.titleA novel homozygous frameshift CCNO variant presenting with primary ciliary dyskinesia and selective IGM deficiency
dc.typeLetter
dspace.entity.typePublication
local.contributor.kuauthorKayalar, Özgecan
local.publication.orgunit1Research Center
local.publication.orgunit2KUTTAM (Koç University Research Center for Translational Medicine)
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relation.isOrgUnitOfPublication.latestForDiscovery91bbe15d-017f-446b-b102-ce755523d939
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