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Genotypic and phenotypic features of mutations in the HINT1 gene among Turkish patients with hereditary axonal neuropathy

dc.contributor.authorParman, Yesim
dc.contributor.authorAcarli, Ayse Ozdag
dc.contributor.authorCakar, Arman
dc.contributor.authorCandayan, Ayse
dc.contributor.authorDurmus, Hacer
dc.contributor.authorCeylaner, Serdar
dc.contributor.authorMatur, Zeliha
dc.contributor.authorOge, Ali
dc.date.accessioned2021-12-10T11:23:53Z
dc.date.available2021-12-10T11:23:53Z
dc.date.issued2021
dc.identifier.citationAcarli A. O. , Cakar A., Candayan A., Durmus H., Ceylaner S., Matur Z., Oge A., Parman Y., "Genotypic and phenotypic features of mutations in the HINT1 gene among Turkish patients with hereditary axonal neuropathy", JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, cilt.26, sa.1, ss.124-125, 2021
dc.identifier.issn1085-9489
dc.identifier.othervv_1032021
dc.identifier.otherav_7b27704c-d96d-4678-b834-3a33ac8bf073
dc.identifier.urihttp://hdl.handle.net/20.500.12627/171815
dc.language.isoeng
dc.subjectSensory Systems
dc.subjectNeurology (clinical)
dc.subjectPhysical Sciences
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectHuman-Computer Interaction
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectNEUROSCIENCES
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectNeurology
dc.subjectDevelopmental Neuroscience
dc.subjectCellular and Molecular Neuroscience
dc.subjectCognitive Neuroscience
dc.subjectGeneral Neuroscience
dc.subjectNeuroscience (miscellaneous)
dc.titleGenotypic and phenotypic features of mutations in the HINT1 gene among Turkish patients with hereditary axonal neuropathy
dc.typeMakale
dc.relation.journalJOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
dc.contributor.departmentİstanbul Teknik Üniversitesi , ,
dc.identifier.volume26
dc.identifier.issue1
dc.identifier.startpage124
dc.identifier.endpage125
dc.contributor.firstauthorID2608187


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