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

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dc.contributor.authorAcarli, Ayse Ozdag
dc.contributor.authorÇAKAR, Arman
dc.contributor.authorCandayan, Ayse
dc.contributor.authorDURMUŞ TEKÇE, Hacer
dc.contributor.authorCeylaner, Serdar
dc.contributor.authorMatur, ZELİHA
dc.contributor.authorOge, Ali
dc.contributor.authorParman, Yesim
dc.contributor.institutionauthorMATUR, ZELİHA
dc.date.accessioned2022-01-13T20:59:49Z
dc.date.available2022-01-13T20:59:49Z
dc.date.issued2021-03-01T00:00:00Z
dc.identifier.citationAcarli A. O. , ÇAKAR A., Candayan A., DURMUŞ TEKÇE 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.urihttp://hdl.handle.net/20.500.12645/30156
dc.identifier.wosWOS:000626893200028
dc.titleGenotypic and phenotypic features of mutations in the HINT1 gene among Turkish patients with hereditary axonal neuropathy
dc.typeArticle
dspace.entity.typePublication
local.avesis.id7b27704c-d96d-4678-b834-3a33ac8bf073
local.publication.isinternational1
relation.isAuthorOfPublication3c69fce6-5ba0-4838-9215-eae7a7125446
relation.isAuthorOfPublication.latestForDiscovery3c69fce6-5ba0-4838-9215-eae7a7125446
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