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Spinocerebellar ataxia type 11.

Giunti, P; Houlden, H; Gardner-Thorpe, C; Worth, PF; Johnson, J; Hilton, DA; Revesz, T; ... Wood, NW; + view all (2012) Spinocerebellar ataxia type 11. In: UNSPECIFIED (pp. 521-534).

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Type: Book chapter
Title: Spinocerebellar ataxia type 11.
DOI: 10.1016/B978-0-444-51892-7.00033-4
Keywords: Age of Onset, Animals, Electrophysiology, Family Health, Female, Humans, Middle Aged, Nerve Tissue Proteins, Neuroimaging, Spinocerebellar Ataxias
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/1271960
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