Novel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrier

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dc.authoridartan, reha/0000-0001-6114-9210
dc.authoridShiraishi, Akira/0000-0003-2184-3587
dc.authorwosidartan, reha/I-6332-2015
dc.contributor.authorShiraishi, Akira
dc.contributor.authorUygun, Vedat
dc.contributor.authorSharfe, Nigel
dc.contributor.authorBeldar, Serap
dc.contributor.authorSun, Mark G. F.
dc.contributor.authorDadi, Harjit
dc.contributor.authorVong, Linda
dc.date.accessioned2024-05-19T14:51:17Z
dc.date.available2024-05-19T14:51:17Z
dc.date.issued2023
dc.departmentİstinye Üniversitesien_US
dc.description.abstract[Abstract Not Available]en_US
dc.identifier.doi10.1182/blood.2022017968
dc.identifier.endpage3230en_US
dc.identifier.issn0006-4971
dc.identifier.issn1528-0020
dc.identifier.issue26en_US
dc.identifier.pmid36745868en_US
dc.identifier.scopus2-s2.0-85150827164en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage3226en_US
dc.identifier.urihttps://doi.org10.1182/blood.2022017968
dc.identifier.urihttps://hdl.handle.net/20.500.12713/5912
dc.identifier.volume141en_US
dc.identifier.wosWOS:001159458800001en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherAmer Soc Hematologyen_US
dc.relation.ispartofBlooden_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.snmz20240519_kaen_US
dc.subjectAciden_US
dc.subjectMalabsorptionen_US
dc.subjectDeficiencyen_US
dc.subjectGeneen_US
dc.titleNovel immunodeficiency caused by homozygous mutation in solute carrier family 19 member 1, which encodes the reduced folate carrieren_US
dc.typeArticleen_US

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