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HARVARD Citation
Van de Vondel, L. et al. (2022). De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia. Movement disorders. 37 (6), pp. 1175-1186. [Online].
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Van de Vondel, L. et al. (2022). De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia. Movement disorders. 37 (6), pp. 1175-1186. [Online].