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

Date

Authors

Hiz, Sahinde Fazilet

Inanir, Busra Elif

Basak, Ayse Nazli

Dogan, Sebahat Nacar

dc.identifier.issn

1353-8020
1873-5126

dc.identifier.doi

10.1016/j.parkreldis.2025.108127

dc.description.volume

142

Publisher

ELSEVIER SCI LTD

DOI

10.1016/j.parkreldis.2025.108127
10.1016/j.parkreldis.2025.108127

Keywords

KIF1C variants , Hereditary spastic paraplegia , Whole exome sequencing , MUTATIONS , PARAPLEGIA , FORM , Clinical Neurology , Neurosciences & Neurology

URI

https://doi.org/10.1016/j.parkreldis.2025.108127
https://openaccess.acibadem.edu.tr/handle/11443/10931

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