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

SLC39A14 mutations expand the spectrum of manganese transporter defects causing parkinsonism-dystonia

Balint, B; Bhatia, KP; (2016) SLC39A14 mutations expand the spectrum of manganese transporter defects causing parkinsonism-dystonia. Movement Disorders , 31 (11) p. 1630. 10.1002/mds.26821.

[thumbnail of Balint_et_al-2016-Movement_Disorders.pdf] Text
Balint_et_al-2016-Movement_Disorders.pdf - Published version
Access restricted to UCL open access staff

Download (95kB)
Type: Article
Title: SLC39A14 mutations expand the spectrum of manganese transporter defects causing parkinsonism-dystonia
DOI: 10.1002/mds.26821
Publisher version: https://doi.org/10.1002/mds.26821
Language: English
Additional information: This version is the version of record. For information on re-use, please refer to the publisher’s terms and conditions.
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 > Department of Neuromuscular Diseases
URI: https://discovery.ucl.ac.uk/id/eprint/10061681
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item