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Delineating the phenotype of autosomal-recessive HPCA mutations: Not only isolated dystonia!

Balint, B; Charlesworth, G; Erro, R; Wood, NW; Bhatia, KP; (2019) Delineating the phenotype of autosomal-recessive HPCA mutations: Not only isolated dystonia! Movement Disorders , 34 (4) pp. 589-592. 10.1002/mds.27638.

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Type: Article
Title: Delineating the phenotype of autosomal-recessive HPCA mutations: Not only isolated dystonia!
DOI: 10.1002/mds.27638
Publisher version: https://doi.org/10.1002/mds.27638
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: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology
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
URI: https://discovery.ucl.ac.uk/id/eprint/10075974
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