Magrinelli, Francesca;
Lohmann, Katja;
(2022)
PRKRAP1 and other pseudogenes in movement disorders: The troublemakers in genetic analyses are more than genomic fossils.
Movement Disorders Clinical Practice
, 9
(5)
pp. 698-702.
10.1002/mdc3.13499.
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| Type: | Article |
|---|---|
| Title: | PRKRAP1 and other pseudogenes in movement disorders: The troublemakers in genetic analyses are more than genomic fossils |
| Open access status: | An open access version is available from UCL Discovery |
| DOI: | 10.1002/mdc3.13499 |
| Publisher version: | https://doi.org/10.1002/mdc3.13499 |
| Language: | English |
| Additional information: | © 2022 The Authors. Movement Disorders Clinical Practice published by Wiley Periodicals LLC. on behalf of International Parkinson and Movement Disorder Society. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
| UCL classification: | 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 > Clinical and Movement Neurosciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology |
| URI: | https://discovery.ucl.ac.uk/id/eprint/10150245 |
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