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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.

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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
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