Recessive Hereditary Methemoglobinemia Type II in a Microcephalic Infant

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dc.contributor.authorBelgemen-Ozer, Tugba
dc.contributor.authorCarman, Kursat Bora
dc.contributor.authorBianchi, Paola
dc.contributor.authorFermo, Elisa
dc.date.accessioned2025-05-10T19:41:22Z
dc.date.issued2024
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstract[No abstract available]
dc.description.sponsorshipDepartment of Medicina Interna
dc.description.sponsorshipThe authors thank Valentina Brancaleone from the Department of Medicina Interna, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy, who performed the molecular study in the beta-globin gene of the patient.
dc.identifier.doi10.1177/00099228241235441
dc.identifier.endpage1640
dc.identifier.issn0009-9228
dc.identifier.issn1938-2707
dc.identifier.issue12
dc.identifier.pmid38439554
dc.identifier.scopus2-s2.0-85187120398
dc.identifier.scopusqualityQ3
dc.identifier.startpage1636
dc.identifier.urihttps://doi.org/10.1177/00099228241235441
dc.identifier.urihttps://hdl.handle.net/20.500.14730/10284
dc.identifier.volume63
dc.identifier.wosWOS:001179648400001
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherSage Publications Inc
dc.relation.ispartofClinical Pediatrics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.titleRecessive Hereditary Methemoglobinemia Type II in a Microcephalic Infant
dc.typeArticle

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