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

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Title:	Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons
Author(s):	Bell, Scott; Rousseau, Justine; Peng, Huashan; Aouabed, Zahia; Priam, Pierre; Theroux, Jean-Francois; Brunner, H.G. ; Ernst, Carl; Campeau, Philippe M.
Publication year:	2019
Source:	American Journal of Human Genetics, vol. 104, iss. 5, (2019), pp. 815-834
ISSN:	0002-9297
DOI:	https://doi.org/10.1016/j.ajhg.2019.03.022
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/203584
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Subject:	All institutes and research themes of the Radboud University Medical Center Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical Neuroscience
Organization:	Human Genetics
Journal title:	American Journal of Human Genetics
Volume:	vol. 104
Issue:	iss. 5
Page start:	p. 815
Page end:	p. 834