Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/18259
DC FieldValueLanguage
dc.contributor.authorErdős, Melindaen_US
dc.contributor.authorMironska, Kristinaen_US
dc.contributor.authorKareva, Lidiaen_US
dc.contributor.authorStavric, Katarinaen_US
dc.contributor.authorHasani, Arijetaen_US
dc.contributor.authorLányi, Árpáden_US
dc.contributor.authorKállai, Juditen_US
dc.contributor.authorMaródi, Lászlóen_US
dc.date.accessioned2022-06-08T08:14:58Z-
dc.date.available2022-06-08T08:14:58Z-
dc.date.issued2022-06-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/18259-
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofPediatric Allergy and Immunologyen_US
dc.titleA novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Projecten_US
dc.typeArticleen_US
dc.identifier.doi10.1111/pai.13805-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/pdf/10.1111/pai.13805-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/full-xml/10.1111/pai.13805-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/pdf/10.1111/pai.13805-
dc.identifier.volume33-
dc.identifier.issue6-
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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