A Homozygous IFNGR1 Mutation Revealed Rare Immunodeficiency Syndrome For A Patient Having Common Symptoms

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dc.contributor.authorSunar, Ilknur
dc.contributor.authorAkalin, Ayse Busra
dc.contributor.authorAkalin, Ibrahim
dc.contributor.authorDemircioglu, Fatih
dc.contributor.authorAlchalabi, Mohammed
dc.contributor.authorDerin, Zeynep
dc.contributor.authorTavil, Betul
dc.date.accessioned2026-04-04T18:55:17Z
dc.date.available2026-04-04T18:55:17Z
dc.date.issued2024
dc.departmentİstanbul Bilgi Üniversitesi
dc.description57th Conference of the European-Society-of-Human-Genetics (ESHG) -- JUN 01-04, 2024 -- Berlin, GERMANY
dc.description.abstract[Abstract Not Available]
dc.description.sponsorshipEuropean Soc Human Genetics
dc.identifier.endpage1032
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.startpage1032
dc.identifier.urihttps://hdl.handle.net/11411/10756
dc.identifier.volume32
dc.identifier.wosWOS:001421430500632
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherSpringernature
dc.relation.ispartofEuropean Journal of Human Genetics
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260402
dc.subject[Keyword Not Available]
dc.titleA Homozygous IFNGR1 Mutation Revealed Rare Immunodeficiency Syndrome For A Patient Having Common Symptoms
dc.typeConference Object

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