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

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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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