eprintid: 10150245
rev_number: 13
eprint_status: archive
userid: 699
dir: disk0/10/15/02/45
datestamp: 2022-06-17 09:24:04
lastmod: 2022-11-21 16:36:07
status_changed: 2022-11-21 16:36:07
type: article
metadata_visibility: show
sword_depositor: 699
creators_name: Magrinelli, Francesca
creators_name: Lohmann, Katja
title: PRKRAP1 and other pseudogenes in movement disorders: The troublemakers in genetic analyses are more than genomic fossils
ispublished: pub
divisions: C07
divisions: F84
divisions: B02
divisions: UCL
divisions: D07
note: © 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.
date: 2022-07
date_type: published
publisher: Wiley
official_url: https://doi.org/10.1002/mdc3.13499
oa_status: green
full_text_type: pub
language: eng
primo: open
primo_central: open_green
verified: verified_manual
elements_id: 1961563
doi: 10.1002/mdc3.13499
lyricists_name: Magrinelli, Francesca
lyricists_id: FMAGR76
actors_name: Bracey, Alan
actors_id: ABBRA90
actors_role: owner
full_text_status: public
publication: Movement Disorders Clinical Practice
volume: 9
number: 5
pagerange: 698-702
citation:        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 <https://doi.org/10.1002/mdc3.13499>.       Green open access   
 
document_url: https://discovery.ucl.ac.uk/id/eprint/10150245/7/Magrinelli_Movement%20Disord%20Clin%20Pract%20-%202022%20-%20Magrinelli%20-%20PRKRAP1%20and%20Other%20Pseudogenes%20in%20Movement%20Disorders%20%20The%20Troublemakers%20in_VoR.pdf