Publication:
DOCK8 Deletions and Mutations Are Associated With The Autosomal Recessive Hyper-IgE Phenotype

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dc.contributor.authorAYDINER, ELİF
dc.contributor.authorsMcGhee, S. A.; Engelhardt, K.; Winkler, S.; Sassi, A.; Woellner, C.; Lopez-Herrera, G.; Chen, A.; Kim, H.; Lloret, M. Garcia; Schulze, I.; Ehl, S.; Thiel, J.; Pfeifer, D.; Veelken, H.; Niehues, T.; Siepermann, K.; Weinspach, S.; Reisli, I.; Keles, S.; Genel, F.; Kutukculer, N.; Camcioglu, Y.; Somer, A.; Karakoc-Aydiner, E.; Barlan, I.
dc.date.accessioned2022-03-12T16:13:37Z
dc.date.accessioned2026-01-11T17:31:15Z
dc.date.available2022-03-12T16:13:37Z
dc.date.issued2010
dc.identifier.doi10.1016/j.jaci.2010.01.006
dc.identifier.issn0091-6749
dc.identifier.urihttps://hdl.handle.net/11424/224963
dc.identifier.wosWOS:000280204100931
dc.language.isoeng
dc.publisherMOSBY-ELSEVIER
dc.relation.ispartofJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleDOCK8 Deletions and Mutations Are Associated With The Autosomal Recessive Hyper-IgE Phenotype
dc.typeconferenceObject
dspace.entity.typePublication
oaire.citation.endPageAB356
oaire.citation.issue2
oaire.citation.startPageAB356
oaire.citation.titleJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
oaire.citation.volume125

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