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The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Broadening the Spectrum of SLC22A5 Phenotype: Primary Carnitine Deficiency Presenting with Focal Myoclonus

Lookup NU author(s): Albert Lim, Dr Dipayan Mitra, Dr Jessica Blickwedel, Dr Anna BasuORCiD

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Publication metadata

Author(s): Khries M, Lim A, Mitra D, Anderson M, Bengtsson J, Bowron A, Harris E, Blickwedel J, Wood K, Basu AP

Publication type: Article

Publication status: Published

Journal: Child Neurology Open

Year: 2023

Volume: 10

Pages: 1-4

Online publication date: 17/07/2023

Acceptance date: 07/06/2023

Date deposited: 09/06/2023

ISSN (electronic): 2329-048X

Publisher: Sage Publications, Inc.

URL: https://doi.org/10.1177/2329048X231184183

DOI: 10.1177/2329048X231184183

ePrints DOI: 10.57711/r0a0-v809


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