Novel De Novo Mutations in KIF1A as a Cause of Hereditary...

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Novel De Novo Mutations in KIF1A as a Cause of Hereditary Spastic Paraplegia With Progressive Central Nervous System Involvement

Hotchkiss, L., Donkervoort, S., Leach, M. E., Mohassel, P., Bharucha-Goebel, D. X., Bradley, N., Nguyen, D., Hu, Y., Gurgel-Giannetti, J., Bo nnemann, C. G.
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Language:
english
Journal:
Journal of Child Neurology
DOI:
10.1177/0883073816639718
Date:
March, 2016
File:
PDF, 484 KB
english, 2016
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