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Screening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy

dc.contributor.authorBATTALOĞLU, ESRA
dc.contributor.authorJordanova, Albena
dc.contributor.authorArmirola-Ricaurte, Camila
dc.contributor.authorde Vriendt, Els
dc.contributor.authorCandayan, Ayse
dc.contributor.authorAsenov, Ognyan
dc.contributor.authorParman, Yesim
dc.contributor.authorChamova, Teodora
dc.contributor.authorTournev, Ivailo
dc.date.accessioned2022-07-04T13:58:22Z
dc.date.available2022-07-04T13:58:22Z
dc.date.issued2022
dc.identifier.citationArmirola-Ricaurte C., de Vriendt E., Candayan A., Asenov O., Parman Y., Chamova T., Tournev I., BATTALOĞLU E., Jordanova A., "Screening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy", EUROPEAN JOURNAL OF HUMAN GENETICS, cilt.30, sa.SUPPL 1, ss.309-310, 2022
dc.identifier.issn1018-4813
dc.identifier.othervv_1032021
dc.identifier.otherav_628be3d9-2e5c-4c3e-953e-a2acfcc0fa12
dc.identifier.urihttp://hdl.handle.net/20.500.12627/183022
dc.language.isoeng
dc.subjectBiochemistry
dc.subjectStructural Biology
dc.subjectGenetics (clinical)
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectGeneral Biochemistry, Genetics and Molecular Biology
dc.subjectBİYOKİMYA VE MOLEKÜLER BİYOLOJİ
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectAging
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectSitogenetik
dc.subjectTemel Bilimler
dc.subjectBiochemistry, Genetics and Molecular Biology (miscellaneous)
dc.subjectGenetics
dc.subjectClinical Biochemistry
dc.subjectCancer Research
dc.subjectMolecular Biology
dc.subjectDrug Discovery
dc.titleScreening of SORD mutations in a CMT cohort expands the clinical spectrum of SORD-related neuropathy
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF HUMAN GENETICS
dc.contributor.departmentVIB UAntwerp Ctr Mol Neurol , ,
dc.identifier.volume30
dc.identifier.issueSUPPL 1
dc.identifier.startpage309
dc.identifier.endpage310
dc.contributor.firstauthorID3416977


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