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Myoclonic dystonia syndrome due to tyrosine hydroxylase deficiency

Stamelou, M; Mencacci, N; Cordivari, C; Batla, A; Houlden, H; Wood, N; Hardy, J; (2012) Myoclonic dystonia syndrome due to tyrosine hydroxylase deficiency. In: (Proceedings) 16th International Congress of Parkinson's Disease and Movement Disorders. (pp. S201-S201). WILEY-BLACKWELL

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Type: Proceedings paper
Title: Myoclonic dystonia syndrome due to tyrosine hydroxylase deficiency
Event: 16th International Congress of Parkinson's Disease and Movement Disorders
Location: Dublin, IRELAND
Dates: 17 June 2012 - 21 June 2012
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
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
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > ION Central Administration
URI: http://discovery.ucl.ac.uk/id/eprint/1404507
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