KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction

Publisher： John Wiley & Sons Inc

E-ISSN： 1531-8249|80|4|633-637

ISSN： 0364-5134

Source： ANNALS OF NEUROLOGY, Vol.80, Iss.4, 2016-10, pp. : 633-637

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