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Inflammatory bowel disease and guillain barre syndrome in FCHO1 deficiency

dc.contributor.authorAydemir, Sezin
dc.contributor.authorİşlek, Ali
dc.contributor.authorNepesov, Serdar
dc.contributor.authorYaman, Yöntem
dc.contributor.authorBaysoy, Gökhan
dc.contributor.authorBeşer, Ömer Faruk
dc.contributor.authorÇullu Çokuğraş, Fügen
dc.contributor.authorBarış, Safa
dc.contributor.authorKarakoç Aydıner, Elif
dc.contributor.authorÇokuğraş, Haluk
dc.contributor.authorHubrack, Satanay Z.
dc.contributor.authorKendir Demirkol, Yasemin
dc.contributor.authorLo, Bernice
dc.contributor.authorKıykım, Ayça
dc.contributor.authorÖzen, Ahmet
dc.date.accessioned2021-10-14T09:48:48Z
dc.date.available2021-10-14T09:48:48Z
dc.date.issued2021en_US
dc.identifier.citationAydemir, S., İşlek, A., Nepesov, S., Yaman, Y., Baysoy, G., Beşer, Ö. F. ... Özen, A. (2021). Inflammatory bowel disease and guillain barre syndrome in FCHO1 deficiency. Journal of Clinical Immunology, 41(6), 1406-1410. https://dx.doi.org/10.1007/s10875-021-01042-2en_US
dc.identifier.issn0271-9142
dc.identifier.issn1573-2592
dc.identifier.urihttps://dx.doi.org/10.1007/s10875-021-01042-2
dc.identifier.urihttps://hdl.handle.net/20.500.12511/8450
dc.description.abstractTo the Editor: FCH And Mu Domain Containing Endocytic Adaptor 1 (FCHO1) gene encodes a protein that plays a critical role in clathrin-mediated endocytosis, a biological process that maintains cellular functions in signaling, nutrient- and growth factor- uptake, and diferentiation [1–3]. Recently, biallelic mutations in FCHO1 were linked to a combined immunodefciency that is characterized by recurrent infections caused by bacteria, viruses, mycobacteria, fungi, T cell lymphopenia, and hypogammaglobulinemia [4, 5].en_US
dc.description.sponsorshipSidra Precision Medicine Programen_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.rightsinfo:eu-repo/semantics/embargoedAccessen_US
dc.subjectFCHO1 Deficiencyen_US
dc.subjectGuillain Barre Syndromeen_US
dc.subjectBowel Diseaseen_US
dc.titleInflammatory bowel disease and guillain barre syndrome in FCHO1 deficiencyen_US
dc.typeeditorialen_US
dc.relation.ispartofJournal of Clinical Immunologyen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalıen_US
dc.authorid0000-0002-4551-5433en_US
dc.authorid0000-0002-9710-8653en_US
dc.identifier.volume41en_US
dc.identifier.issue6en_US
dc.identifier.startpage1406en_US
dc.identifier.endpage1410en_US
dc.relation.publicationcategoryDiğeren_US
dc.identifier.doi10.1007/s10875-021-01042-2en_US
dc.identifier.wosqualityQ1en_US
dc.identifier.scopusqualityQ1en_US


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