Cite
HARVARD Citation
Manole, A. et al. (2017). De novo KCNA2 mutations cause hereditary spastic paraplegia. Annals of neurology. 81 (2), pp. 326-328. [Online].
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Manole, A. et al. (2017). De novo KCNA2 mutations cause hereditary spastic paraplegia. Annals of neurology. 81 (2), pp. 326-328. [Online].