Selcuk, E. Et Al. 2022. MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia. MOLECULAR GENETICS AND GENOMICS , vol.297, no.4 , 1141-1150.

Selcuk, E., Kirimtay, K., Temizci İmanç, B., Akarsu, Ş., Everest, E., Baslo, M. B., ... DEMİRKIRAN, D. M.(2022). MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia. MOLECULAR GENETICS AND GENOMICS , vol.297, no.4, 1141-1150.

Selcuk, Ece Et Al. "MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia," MOLECULAR GENETICS AND GENOMICS , vol.297, no.4, 1141-1150, 2022

Selcuk, Ece Et Al. "MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia." MOLECULAR GENETICS AND GENOMICS , vol.297, no.4, pp.1141-1150, 2022

Selcuk, E. Et Al. (2022) . "MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia." MOLECULAR GENETICS AND GENOMICS , vol.297, no.4, pp.1141-1150.

@article{article, author={Ece Selcuk Et Al. }, title={MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia}, journal={MOLECULAR GENETICS AND GENOMICS}, year=2022, pages={1141-1150} }