Yucel-Yilmaz, D. Et Al. 2018. Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span. BRAIN & DEVELOPMENT , vol.40, no.6 , 458-464.

Yucel-Yilmaz, D., Yucesan, E., YALNIZOĞLU, D., Oguz, K. K., Sagiroglu, M. S., Ozbek, U., ... Serdaroglu, E.(2018). Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span. BRAIN & DEVELOPMENT , vol.40, no.6, 458-464.

Yucel-Yilmaz, DİDEM Et Al. "Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span," BRAIN & DEVELOPMENT , vol.40, no.6, 458-464, 2018

Yucel-Yilmaz, DİDEM Y. Et Al. "Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span." BRAIN & DEVELOPMENT , vol.40, no.6, pp.458-464, 2018

Yucel-Yilmaz, D. Et Al. (2018) . "Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span." BRAIN & DEVELOPMENT , vol.40, no.6, pp.458-464.

@article{article, author={DİDEM YÜCEL YILMAZ Et Al. }, title={Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span}, journal={BRAIN & DEVELOPMENT}, year=2018, pages={458-464} }