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Paroxysmal, exercise-induced, diurnally fluctuating dystonia: Expanding the phenotype of SPG8.

Mulroy, E; Magrinelli, F; Mohd Fauzi, NA; Kutty, SK; Latorre, A; Bhatia, KP; (2021) Paroxysmal, exercise-induced, diurnally fluctuating dystonia: Expanding the phenotype of SPG8. Parkinsonism & Related Disorders , 85 pp. 26-28. 10.1016/j.parkreldis.2021.02.011. Green open access

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Type: Article
Title: Paroxysmal, exercise-induced, diurnally fluctuating dystonia: Expanding the phenotype of SPG8.
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.1016/j.parkreldis.2021.02.011
Publisher version: https://doi.org/10.1016/j.parkreldis.2021.02.011
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: Glut1 Deficiency Syndrome, Hereditary, Parkinson Disease, Spastic Paraplegia, Wiskott-Aldrich Syndrome Protein
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Clinical and Movement Neurosciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Clinical Neuroscience
URI: https://discovery.ucl.ac.uk/id/eprint/10124487
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