Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons

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Publication year
2019
Author(s)
Bell, Scott
Rousseau, Justine
Peng, Huashan
Aouabed, Zahia
Priam, Pierre
Theroux, Jean-Francois
Brunner, H.G.
Ernst, Carl
Campeau, Philippe M.
Source
American Journal of Human Genetics, 104, 5, (2019), pp. 815-834
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DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/203584   https://hdl.handle.net/2066/203584
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