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).
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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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