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

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.accessioned2021-06-10T19:38:30Z
dc.date.available2021-06-10T19:38:30Z
dc.date.issued2021
dc.identifier.issn1085-9489
dc.identifier.issn1529-8027
dc.identifier.urihttp://hdl.handle.net/11446/4355
dc.descriptionWOS:000626893200028en_US
dc.description.abstract[No Abstract Available]en_US
dc.description.abstract427en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHINT1en_US
dc.subjectneuromyotoniaen_US
dc.subjectfebril seizureen_US
dc.subjectaxonal neuropathyen_US
dc.titleGenotypic and phenotypic features of mutations in the HINT1 gene among Turkish patients with hereditary axonal neuropathyen_US
dc.typeconferenceObjecten_US
dc.relation.journalJournal Of The Peripheral Nervous Systemen_US
dc.department[0-Belirlenecek]en_US
dc.identifier.issue1en_US
dc.identifier.volume26en_US
dc.identifier.startpage124en_US
dc.identifier.endpage125en_US
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanıen_US
dc.institutionauthor[0-Belirlenecek]
dc.department-temp[Acarli, Ayse Ozdag; Cakar, Arman; Durmus, Hacer; Oge, Ali; Parman, Yesim] Istanbul Univ, Dept Neurol, Istanbul Fac Med, Istanbul, Turkey; [Candayan, Ayse] Bogazici Univ, Dept Mol Biol & Genet, Istanbul, Turkey; [Matur, Zeliha] Bilim Univ, Istanbul, Turkeyen_US


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