Cite
HARVARD Citation
Hong, D. et al. (2019). A novel CPT1C variant causes pure hereditary spastic paraplegia with benign clinical course. Annals of clinical and translational neurology. 6 (3), pp. 610-614. [Online].
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Hong, D. et al. (2019). A novel CPT1C variant causes pure hereditary spastic paraplegia with benign clinical course. Annals of clinical and translational neurology. 6 (3), pp. 610-614. [Online].