UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

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.

[img] Text
Bhatia HPCA dystonia delineating the phenotype_Balint et al final.pdf - Accepted version
Access restricted to UCL open access staff

Download (707kB)
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 > Provost and Vice Provost Offices
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
Downloads since deposit
1Download
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item