Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span

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dc.contributor.authorYucel\\-Yilmaz, Didem
dc.contributor.authorYucesan, Emrah
dc.contributor.authorYalnizoglu, Dilek
dc.contributor.authorOguz, Kader Karli
dc.contributor.authorSagiroglu, Mahmut Samil
dc.contributor.authorOzbek, Ugur
dc.contributor.authorSerdaroglu, Esra
dc.contributor.authorBilgic, Basar
dc.contributor.authorErdem, Sevim
dc.contributor.authorIseri, Sibel Aylin Ugur
dc.contributor.authorHanagasi, Hasmet
dc.contributor.authorGurvit, Hakan
dc.contributor.authorOzgul, Riza Kaksal
dc.contributor.authorDursun, Ali
dc.date.accessioned2025-10-16T15:25:31Z
dc.date.issued2018
dc.identifier.doi10.1016/j.braindev.2018.02.013
dc.identifier.otherWOS:000433997300003
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/8263
dc.publisherELSEVIER SCIENCE BV
dc.sourceBRAIN \& DEVELOPMENT
dc.subjectKIFIC
dc.subjectHereditary spastic paraplegia
dc.subjectAtaxia
dc.subjectKinesin
dc.titleClinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span
dc.typeArticle

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