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STXBP1 stop‐loss mutation associated with complex early onset movement disorder without epilepsy

Spaull, Robert; Steel, Dora; Barwick, Katy; Prabhakar, Prab; Wakeling, Emma; Kurian, Manju A; (2022) STXBP1 stop‐loss mutation associated with complex early onset movement disorder without epilepsy. Movement Disorders Clinical Practice 10.1002/mdc3.13509. (In press). Green open access

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Type: Article
Title: STXBP1 stop‐loss mutation associated with complex early onset movement disorder without epilepsy
Open access status: An open access version is available from UCL Discovery
DOI: 10.1002/mdc3.13509
Publisher version: https://doi.org/10.1002/mdc3.13509
Language: English
Additional information: Copyright © 2022 The Authors. This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health > Developmental Neurosciences Dept
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Population Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
URI: https://discovery.ucl.ac.uk/id/eprint/10150791
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