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Phenotypic variability in a dystonia family with mutations in the manganese transporter gene

Delnooz, CCS; Wevers, RA; Quadri, M; Clayton, PT; Mills, PB; Tuschl, K; Steenbergen, EJ; ... van de Warrenburg, BPC; + view all (2013) Phenotypic variability in a dystonia family with mutations in the manganese transporter gene. MOVEMENT DISORDERS , 28 (5) pp. 685-686. 10.1002/mds.25390.

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Type: Article
Title: Phenotypic variability in a dystonia family with mutations in the manganese transporter gene
DOI: 10.1002/mds.25390
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, POLYCYTHEMIA, SLC30A10, HYPERMANGANESEMIA
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 Life Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences > Cell and Developmental Biology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > UCL GOS Institute of Child Health
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Pop Health Sciences > UCL GOS Institute of Child Health > ICH Genetics and Genomic Medicine Prog
URI: http://discovery.ucl.ac.uk/id/eprint/1392537
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