A Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiency

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dc.authoridNG, YUK YIN/0000-0001-9755-6045|Baris, Safa/0000-0002-4730-9422|Kiykim, Ayca/0000-0001-5821-3963|Akcay, Arzu/0000-0001-8343-1153|OZEN, AHMET/0000-0002-9065-1901|Firtina, Sinem/0000-0002-3370-8545|Aydin Sayitoglu, Muge/0000-0002-8648-213X
dc.authorwosidFırtına, Sinem/GSD-3891-2022
dc.authorwosidNG, YUK YIN/AAG-7977-2020
dc.authorwosidBaris, Safa/AAH-1932-2019
dc.authorwosidSayitoglu, Muge/B-6578-2015
dc.authorwosidKiykim, Ayca/J-6400-2017
dc.authorwosidAkcay, Arzu/ABH-4540-2020
dc.authorwosidOZEN, AHMET/R-6749-2017
dc.contributor.authorFirtina, Sinem
dc.contributor.authorCipe, Funda
dc.contributor.authorNg, Yuk Yin
dc.contributor.authorKiykim, Ayca
dc.contributor.authorNg, Ozden Hatirnaz
dc.contributor.authorSudutan, Tugce
dc.contributor.authorAydogmus, Cigdem
dc.date.accessioned2024-07-18T20:42:13Z
dc.date.available2024-07-18T20:42:13Z
dc.date.issued2019
dc.departmentİstanbul Bilgi Üniversitesien_US
dc.description.abstract[Abstract Not Available]en_US
dc.description.sponsorshipIstanbul University Research Fund [52575, 20499]en_US
dc.description.sponsorshipThis project is supported by Istanbul University Research Fund (No: 52575 and 20499) and Istanbul Bilgi University [Y.Y Ng, 2017)].en_US
dc.identifier.doi10.1007/s10875-019-00615-6
dc.identifier.endpage147en_US
dc.identifier.issn0271-9142
dc.identifier.issn1573-2592
dc.identifier.issue2en_US
dc.identifier.pmid30903456en_US
dc.identifier.scopus2-s2.0-85063998040en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage144en_US
dc.identifier.urihttps://doi.org/10.1007/s10875-019-00615-6
dc.identifier.urihttps://hdl.handle.net/11411/7182
dc.identifier.volume39en_US
dc.identifier.wosWOS:000463216500006en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherSpringer/Plenum Publishersen_US
dc.relation.ispartofJournal of Clinical Immunologyen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectMutationen_US
dc.subjectGeneen_US
dc.subjectDeficiencyen_US
dc.titleA Novel FOXN1 Variant Is Identified in Two Siblings with Nude Severe Combined Immunodeficiencyen_US
dc.typeLetteren_US

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