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THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations

Xiromerisiou, G; Houlden, H; Scarmeas, N; Stamelou, M; Kara, E; Hardy, J; Lees, AJ; ... Bhatia, KP; + view all (2012) THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations. MOVEMENT DISORDERS , 27 (10) pp. 1290-1294. 10.1002/mds.25146.

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Type: Article
Title: THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations
DOI: 10.1002/mds.25146
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, THAP1, dystonia, DYT6, mutations, phenotype, genotype, DOPA-RESPONSIVE DYSTONIA, PRIMARY TORSION DYSTONIA, EARLY-ONSET DYSTONIA, DYT6 PRIMARY DYSTONIA, SEQUENCE VARIANTS, GENE DYT1, LOCUS, IDENTIFICATION, FAMILY, PARKINSONISM
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 > Neurodegenerative Diseases
URI: http://discovery.ucl.ac.uk/id/eprint/1356962
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