Early‐Onset Movement Disorder Syndrome Caused by Biallelic Variants in PDE1B Encoding Phosphodiesterase 1B

Poleg, T., Hadar, N., Kristal, E. et al. (19 more authors) (2025) Early‐Onset Movement Disorder Syndrome Caused by Biallelic Variants in PDE1B Encoding Phosphodiesterase 1B. Movement Disorders. ISSN 0885-3185

Abstract

Metadata

Item Type: Article
Authors/Creators:
  • Poleg, T.
  • Hadar, N.
  • Kristal, E.
  • Roberts, N.Y.
  • Dolgin, V.
  • Aminov, I.
  • Safran, A.
  • Agam, N.
  • Jean, M.
  • Freund, O.
  • Sheridan, E.G.
  • Poulter, J.A. ORCID logo https://orcid.org/0000-0003-2048-5693
  • Thompson, M.L.
  • Algoos, Y.
  • Al-Qahtani, S.
  • AlAbdi, L.
  • Maddirevula, S.
  • Hartill, V.
  • Houlden, H.
  • Maroofian, R.
  • Nahum, A.
  • Birk, O.S.
Copyright, Publisher and Additional Information:

© 2025 The Author(s). This is an open access article under the terms of the Creative Commons Attribution License (CC-BY 4.0), which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited.

Keywords: PDE1B; movement disorder; phosphodies-terase; exome sequencing; early onset
Dates:
  • Accepted: 12 May 2025
  • Published (online): 10 June 2025
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds)
Funding Information:
Funder
Grant number
UKRI (UK Research and Innovation)
MR/Y034325/1
Rosetrees Trust
A2459
Depositing User: Symplectic Publications
Date Deposited: 30 Jun 2025 12:51
Last Modified: 30 Jun 2025 12:51
Status: Published
Publisher: Wiley
Identification Number: 10.1002/mds.30249
Related URLs:
Open Archives Initiative ID (OAI ID):

Export

Statistics