Correction to: Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye (Journal of Clinical Immunology, (2024), 44, 7, (157), 10.1007/s10875-024-01759-w)

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dc.contributor.authorErman, Baran
dc.contributor.authorAba, Ümran
dc.contributor.authorİpşir, Canberk
dc.contributor.authorPehlivan, Damla
dc.contributor.authorAytekin, Caner
dc.contributor.authorÇildir, Gökhan
dc.contributor.authorÇiçek, Begüm
dc.contributor.authorBozkurt, Ceren
dc.contributor.authorTekeoğlu, Sidem
dc.contributor.authorKaya, Melisa
dc.contributor.authorAydoğmuş, Çiğdem
dc.contributor.authorÇipe, Funda
dc.contributor.authorSucak, Gülsan
dc.contributor.authorEltan, Sevgi Bilgiç
dc.contributor.authorÖzen, Ahmet
dc.contributor.authorBarış, Safa
dc.contributor.authorKarakoç-Aydıner, Elif
dc.contributor.authorKıykım, Ayça
dc.contributor.authorKaraatmaca, Betül
dc.contributor.authorKöse, Hülya
dc.contributor.authorKocacık Uygun, Dilara Fatma
dc.contributor.authorÇelmeli, Fatih
dc.contributor.authorArıkoğlu, Tuğba
dc.contributor.authorÖzcan, Dilek
dc.contributor.authorKeskin, Özlem
dc.contributor.authorArık, Elif
dc.contributor.authorSoyak Aytekin, Elif
dc.contributor.authorCesur, Mahmut
dc.contributor.authorKüçükosmanoğlu, Ercan
dc.contributor.authorKılıç, Mehmet
dc.contributor.authorYüksek, Mutlu
dc.contributor.authorBıçakçı, Zafer
dc.contributor.authorEsenboğa, Saliha
dc.contributor.authorAyvaz, Deniz Çağdaş
dc.contributor.authorSefer, Asena Pınar
dc.contributor.authorGüner, Şükrü Nail
dc.contributor.authorKeleş, Sevgi
dc.contributor.authorReisli, İsmail
dc.contributor.authorMuşabak, Uğur
dc.contributor.authorDeveci Demirbaş, Nazlı
dc.contributor.authorHaskoloğlu, Şule
dc.contributor.authorKılıç, Sara Şebnem
dc.contributor.authorMetin, Ayşe
dc.contributor.authorDoğu, Figen
dc.contributor.authorİkincioğulları, Aydan
dc.contributor.authorTezcan, İlhan
dc.date.accessioned2024-12-04T12:24:47Z
dc.date.available2024-12-04T12:24:47Z
dc.date.issued2025en_US
dc.departmentFakülteler, Tıp Fakültesien_US
dc.description.abstractSince the publication of this article we have noticed several errors within the main Table 1 of the manuscript. Four variants were given with different transcript IDs of the same gene. There are also 2 nomenclature errors in the variants of P58 and P117. The necessary corrections have been made in the table below. The errors do not affect the causality of the variants, the results or conclusions reported in the manuscript. The authors apologize for the error, and regret any inconvenience this may have caused. The original version has been corrected. (Table presented.) Patient no Clinical diagnosis (IUIS) Age Gender Consan Gene Variant Transcript ID Zygosity Consequence Novelty P18 CID 20 F + c.214G>A p.Gly72Ser NM_001199917.1 The true RefseqID should be NM_001199919.1 Hom Missense Novel P29 SCID 6 m F + c.551_555del p.Glu184Glyfs*2 c.241G>A p.Gly81Arg NM_000022.4 NM_000022.4 The true RefseqID should be NM_001322050 for these variants Comp. Het Out of frame/Deletion Missense Novel rs2065384316 P34 SCID 1 M + c.779A>G p.Glu260Gly NM_001322050 The true RefseqID should be NM_000022.4 for this variant Hom Missense rs1354071013 P58 SCID 2 M + c.1633delT p.Glu545AsnfsTer The correct nomenclature of this variant is c.1633del p.Glu545Asnfs*58 NM_001350965.2 Hom Out of frame/Deletion Novel P113 PAD/CVID 7 F + c.919C>T p.Arg307Trp NM_001372051.1 The true RefseqID should be NM_001080125.1 Hom Missense rs17860424 P117 SCID 1 F + c.2322G>A p.Arg737His The correct nomenclature of this variant is c.2210G>A p.Arg737His The nucleotide position 2322 refers an old transcript NM_000448.3 Hom Missense rs104894286en_US
dc.identifier.citationErman, B., Aba, Ü., İpşir, C., Pehlivan, D., Aytekin, C., Çildir, G., Çiçek, B., Bozkurt, C., Tekeoğlu, S., Kaya, M., Aydoğmuş, Ç, Çipe, F., Sucak, G., Eltan, S. B., Özen, A., Barış, S., Karakoç-Aydıner, E., Kıykım, A., Karaatmaca, B., Köse, H., Kocacık Uygun, D. F., Çelmeli, F., Arıkoğlu, T., Özcan, D., Keskin, Ö., Arık, E., Soyak Aytekin, E., Cesur, M., Küçükosmanoğlu, E., Kılıç, M., Yüksek, M., Bıçakçı, Z., Esenboğa, S., Ayvaz, D. Ç., Sefer, A. P., Güner, Ş. N., Keleş, S., Reisli, İ., Musabak, U., Demirbaş, N. D., Haskoloğlu, Ş., Kılıç, S. Ş., Metin, A., Doğu, F., İkincioğulları, A., Tezcan, İ. (2025). Correction to: Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye (Journal of Clinical Immunology, (2024), 44, 7, (157), 10.1007/s10875-024-01759-w), Journal of Clinical Immunology, 45(1). 10.1007/s10875-024-01841-3en_US
dc.identifier.issn0271-9142
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-85197307217
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://hdl.handle.net/20.500.12939/5065
dc.identifier.volume45en_US
dc.indekslendigikaynakScopus
dc.institutionauthorÇipe, Funda
dc.language.isoen
dc.publisherSpringeren_US
dc.relation.ispartofJournal of Clinical Immunology
dc.relation.isversionof10.1007/s10875-024-01759-wen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCase reporten_US
dc.subjectClinical articleen_US
dc.subjectErratumen_US
dc.subjectEtiologyen_US
dc.subjectFemaleen_US
dc.subjectHumanen_US
dc.subjectDiagnosisen_US
dc.subjectMaleen_US
dc.subjectSchool childen_US
dc.titleCorrection to: Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye (Journal of Clinical Immunology, (2024), 44, 7, (157), 10.1007/s10875-024-01759-w)
dc.typeOther

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