Publication:
THE PHENOTYPE - GENOTYPE RELATIONSHIP IN SEVERE CONGENITAL NEUTROPENIA PATIENTS

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dc.contributor.authorsBaris, Safa; Karakoc-Aydiner, Elif; Kiykim, Ayca; Cagan, Havva Hasret; Boztug, Kaan; Barlan, Isil B.
dc.date.accessioned2022-03-12T16:14:48Z
dc.date.accessioned2026-01-11T07:21:44Z
dc.date.available2022-03-12T16:14:48Z
dc.date.issued2014
dc.identifier.doidoiWOS:000341839800161
dc.identifier.eissn1573-2592
dc.identifier.issn0271-9142
dc.identifier.urihttps://hdl.handle.net/11424/225469
dc.identifier.wosWOS:000341839800161
dc.language.isoeng
dc.publisherSPRINGER/PLENUM PUBLISHERS
dc.relation.ispartofJOURNAL OF CLINICAL IMMUNOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectKostman disease
dc.subjectsevere congenital neutropenia
dc.subjectHAX1
dc.subjectG6PC3
dc.titleTHE PHENOTYPE - GENOTYPE RELATIONSHIP IN SEVERE CONGENITAL NEUTROPENIA PATIENTS
dc.typeconferenceObject
dspace.entity.typePublication
oaire.citation.endPage745
oaire.citation.issue6
oaire.citation.startPage744
oaire.citation.titleJOURNAL OF CLINICAL IMMUNOLOGY
oaire.citation.volume34

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