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Brief CommunicationKIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction
Jessica Duis MD, MS,  Shannon Dean MD, PhD,  Carolyn Applegate MGC, CGC,  Amy Harper MD,  Rui Xiao PhD,  Weimin He PhD,  James D. Dollar MD,  Lisa R. Sun MD,  Marta Biderman Waberski MD,  Thomas O. Crawford MD,  Ada Hamosh MD, MPH,  Carl E. Stafstrom MD, PhD, 

How to cite

Duis, J., Dean, S., Applegate, C., Harper, A., Xiao, R., He, W., Dollar, J.D., Sun, L.R., Waberski, M.B., Crawford, T.O., Hamosh, A. and Stafstrom, C.E. (2016), KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction. Ann Neurol., 80: 633-637. https://doi.org/10.1002/ana.24744

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