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

Yücel-Yılmaz, DYücesan, EmrahYalnızoğlu, DOğuz, KKSağıroğlu, MŞÖzbek, USerdaroğlu, EBilgiç, BErdem, Sİşeri, SAUHanağası, HGürvit, HÖzgül, RKDursun, A2020-01-142020-01-142018-06-01Yücel-Yılmaz D., Yücesan E., Yalnızoğlu D., Oğuz K., Sağıroğlu M., Özbek U., Serdaroğlu E., Bilgiç B., Erdem S., İşeri S., et al., -Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.-, Brain & development, cilt.40, ss.458-464, 2018https://openaccess.bezmialem.edu.tr/handle/20.500.12645/12732Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span.ArticleWOS:0004339973000038504345616010.1016/j.braindev.2018.02.013