Cite
HARVARD Citation
Gauthier, J. et al. (2018). Recessive mutations in >VPS13D cause childhood onset movement disorders. Annals of neurology. 83 (6), pp. 1089-1095. [Online].
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Gauthier, J. et al. (2018). Recessive mutations in >VPS13D cause childhood onset movement disorders. Annals of neurology. 83 (6), pp. 1089-1095. [Online].