Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease

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dc.contributor.authorRavell Juan C
dc.contributor.authorMatsuda-Lennikov Mami
dc.contributor.authorChauvin Samuel D
dc.contributor.authorZou Juan
dc.contributor.authorBiancalana Matthew
dc.contributor.authorDeeb Sally J
dc.contributor.authorPrice Susan
dc.contributor.authorPrice Susan
dc.contributor.authorNotarangelo Giulia
dc.contributor.authorJiang Ping
dc.contributor.authorMorawski Aaron
dc.contributor.authorBinder Kyle W
dc.contributor.authorMukherjee Ratnadeep
dc.contributor.authorAnibal James T
dc.contributor.authorSellers Brian
dc.contributor.authorZheng Lixin
dc.contributor.authorHe Tingyan
dc.contributor.authorGeorge Alex
dc.contributor.authorPittaluga Stefania
dc.contributor.authorPowers Astin
dc.contributor.authorKleiner David E
dc.contributor.authorKapuria Devika
dc.contributor.authorGhany Marc
dc.contributor.authorHunsberger Sally
dc.contributor.authorCohen Jeffrey I
dc.contributor.authorUzel Gulbu
dc.contributor.authorBergerson Jenna
dc.contributor.authorWolfe Lynne
dc.contributor.authorToro Camilo
dc.contributor.authorGahl William
dc.contributor.authorFolio Les R
dc.contributor.authorMatthews Helen
dc.contributor.authorAngelus Pam
dc.contributor.authorChinn Ivan K
dc.contributor.authorOrange Jordan S
dc.contributor.authorTrujillo-Vargas Claudia M
dc.contributor.authorFranco Jose Luis
dc.contributor.authorOrrego-Arango Julio
dc.contributor.authorGutiérrez-Hincapié Sebastian
dc.contributor.authorPatel Niraj Chandrakant
dc.contributor.authorRaymond Kimiyo
dc.contributor.authorPATIROĞLU TÜRKAN
dc.contributor.authorÜNAL EKREM
dc.contributor.authorKARAKÜKCÜ MUSA
dc.contributor.authorDay Alexandre GR
dc.contributor.authorMehta Pankaj
dc.contributor.authorMasutani Evan
dc.contributor.authorDe Ravin Suk
dc.contributor.authorMalech Harry L
dc.contributor.authorAltan-Bonnet Grégoire
dc.contributor.authorRao V Koneti
dc.contributor.authorMann Matthias
dc.contributor.authorLenardo Michael J
dc.contributor.authorÜnal, Ekrem
dc.date.accessioned2026-06-12T11:49:00Z
dc.date.issued2020
dc.descriptionSCI-Expanded | YÖK-Özgeçmiş
dc.identifier.doi10.1172/JCI131116
dc.identifier.issn0021-9738
dc.identifier.urihttps://hdl.handle.net/20.500.11782/5871
dc.relation.ispartofJournal of Clinical Investigation
dc.titleDefective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease
dspace.entity.typePublication
relation.isAuthorOfPublicationcd35ec05-b9b3-4f63-a13f-bc9dc6344971
relation.isAuthorOfPublication.latestForDiscoverycd35ec05-b9b3-4f63-a13f-bc9dc6344971

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