Van de Vondel, L. Et Al. 2022. De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia. MOVEMENT DISORDERS , vol.37, no.6 , 1175-1186.

Van de Vondel, L., De Winter, J., Beijer, D., Coarelli, G., Wayand, M., Palvadeau, R., ... Pauly, M. G.(2022). De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia. MOVEMENT DISORDERS , vol.37, no.6, 1175-1186.

Van de Vondel, Liedewei Et Al. "De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia," MOVEMENT DISORDERS , vol.37, no.6, 1175-1186, 2022

Van de Vondel, Liedewei V. Et Al. "De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia." MOVEMENT DISORDERS , vol.37, no.6, pp.1175-1186, 2022

Van de Vondel, L. Et Al. (2022) . "De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia." MOVEMENT DISORDERS , vol.37, no.6, pp.1175-1186.

@article{article, author={Liedewei Van de Vondel Et Al. }, title={De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia}, journal={MOVEMENT DISORDERS}, year=2022, pages={1175-1186} }