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Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity

Hammer, MB; Eleuch-Fayache, G; Schottlaender, LV; Nehdi, H; Gibbs, JR; Arepalli, SK; Chong, SB; ... Singleton, AB; + view all (2013) Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity. AMERICAN JOURNAL OF HUMAN GENETICS , 92 (2) pp. 245-251. 10.1016/j.ajhg.2012.12.012.

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Type: Article
Title: Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity
DOI: 10.1016/j.ajhg.2012.12.012
Keywords: Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, BETA-GLUCOSIDASE-2, DISEASE
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 > Department of Neuromuscular Diseases
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 Developmental Neurosciences Prog
URI: http://discovery.ucl.ac.uk/id/eprint/1390080
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