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Two homozygous KIF1C variants in a Turkish family presenting with cerebellar dysfunction and spastic paraparesis with MRI findings

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dc.contributor.authorTarhan, Gullu
dc.contributor.authorHiz, Sahinde Fazilet
dc.contributor.authorInanir, Busra Elif
dc.contributor.authorSimsir, Gulsah
dc.contributor.authorTekgul, Seyma
dc.contributor.authorBasak, Ayse Nazli
dc.contributor.authorDogan, Sebahat Nacar
dc.date.accessioned2026-11-05T11:02:32Z
dc.date.issued2026
dc.description.pages108127
dc.description.volume142
dc.identifier.doi10.1016/j.parkreldis.2025.108127
dc.identifier.issn1353-8020
dc.identifier.issn1873-5126
dc.identifier.urihttps://doi.org/10.1016/j.parkreldis.2025.108127
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/10931
dc.identifier.wosWOS:001632752200002
dc.language.isoen
dc.publisherELSEVIER SCI LTD
dc.relation.hasversion10.1016/j.parkreldis.2025.108127
dc.relation.ispartofPARKINSONISM & RELATED DISORDERS
dc.subjectKIF1C variants
dc.subjectHereditary spastic paraplegia
dc.subjectWhole exome sequencing
dc.subjectMUTATIONS
dc.subjectPARAPLEGIA
dc.subjectFORM
dc.subjectClinical Neurology
dc.subjectNeurosciences & Neurology
dc.titleTwo homozygous KIF1C variants in a Turkish family presenting with cerebellar dysfunction and spastic paraparesis with MRI findings
dc.typeEditorial Material
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.volume142
person.identifier.orcid0000-0001-6587-0101
person.identifier.ridAAS-1939-2020
person.identifier.ridIAR-0087-2023

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