RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity

Maroofian, R. orcid.org/0000-0001-6763-1542, Sarraf, P., O’Brien, T.J. et al. (29 more authors) (2024) RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity. Brain, 147 (7). pp. 2334-2343. ISSN 0006-8950

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Item Type: Article
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© The Author(s) 2024. Published by Oxford University Press on behalf of the Guarantors of Brain. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

Keywords: dHMN; hereditary spastic paraplegia; neurodegeneration; polyneuropathy; Humans; Male; Female; Child; Adult; Adolescent; Young Adult; Middle Aged; Animals; Pedigree; Lower Extremity; Caenorhabditis elegans; Muscle Spasticity; Spastic Paraplegia, Hereditary; Mutation
Dates:
  • Published: July 2024
  • Published (online): 25 March 2024
  • Accepted: 25 February 2024
  • Submitted: 30 August 2023
Institution: The University of Sheffield
Academic Units: The University of Sheffield > Faculty of Medicine, Dentistry and Health (Sheffield) > School of Medicine and Population Health
Depositing User: Symplectic Sheffield
Date Deposited: 04 Sep 2024 11:37
Last Modified: 04 Sep 2024 11:37
Status: Published
Publisher: Oxford University Press (OUP)
Refereed: Yes
Identification Number: 10.1093/brain/awae091
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