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

Lookup NU author(s): Dr 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).

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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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