A43 Intrinsic mutant HTT-mediated defects in oligodendroglia cells contribute to myelin deficits and behavioural abnormalities in huntington disease | Journal of Neurology, Neurosurgery & Psychiatry

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Pathogenic mechanisms

A43 Intrinsic mutant HTT-mediated defects in oligodendroglia cells contribute to myelin deficits and behavioural abnormalities in huntington disease

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Cite this article as:: Bardile CF, Garcia-Miralles M, Caron N, et al

A43 Intrinsic mutant HTT-mediated defects in oligodendroglia cells contribute to myelin deficits and behavioural abnormalities in huntington disease

Journal of Neurology, Neurosurgery & Psychiatry 2018;89:A15-A16.