Cite
HARVARD Citation
Duis, J. et al. (n.d.). KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction. Annals of neurology. 80 (4), pp. 633-637. [Online].
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Duis, J. et al. (n.d.). KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction. Annals of neurology. 80 (4), pp. 633-637. [Online].