IRF2BPL mutations cause autosomal dominant dystonia with anarthria, slow saccades and seizures

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IRF2BPL mutations cause autosomal dominant dystonia with anarthria, slow saccades and seizures

Ganos, C; Zittel, S; Hidding, U; Funke, C; Biskup, S; Bhatia, KP; (2019) IRF2BPL mutations cause autosomal dominant dystonia with anarthria, slow saccades and seizures. Parkinsonism & Related Disorders , 68 pp. 57-59. 10.1016/j.parkreldis.2019.09.020. Green open access

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Type:	Article
Title:	IRF2BPL mutations cause autosomal dominant dystonia with anarthria, slow saccades and seizures
Location:	England
Open access status:	An open access version is available from UCL Discovery
DOI:	10.1016/j.parkreldis.2019.09.020
Publisher version:	https://doi.org/10.1016/j.parkreldis.2019.09.020
Language:	English
Additional information:	This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords:	Anarthria, Aphonia, Dystonia, IRF2BPL, Seizures
UCL classification:	UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Clinical and Movement Neurosciences
URI:	https://discovery.ucl.ac.uk/id/eprint/10085119

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