UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure.

Guerrero-López, R; García-Ruiz, PJ; Giráldez, BG; Durán-Herrera, C; Querol-Pascual, MR; Ramírez-Moreno, JM; Más, S; (2012) A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure. Mov Disord , 27 (14) pp. 1826-1827. 10.1002/mds.25114.

Full text not available from this repository.
Type: Article
Title: A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure.
Location: United States
DOI: 10.1002/mds.25114
Keywords: Adult, Ataxia, Female, Humans, Lysosome-Associated Membrane Glycoproteins, Mutation, Myoclonic Epilepsies, Progressive, Myoclonus, Receptors, Scavenger, Renal Insufficiency, Sequence Analysis, DNA
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/1413045
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item