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Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus

Blauwendraat, C; Bras, JM; Nalls, MA; Lewis, PA; Hernandez, DG; Singleton, AB; International Parkinson's Disease Genomics Consortium; (2018) Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus. Movement Disorders 10.1002/mds.103. (In press). Green open access

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Type: Article
Title: Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1002/mds.103
Publisher version: http://doi.org/10.1002/mds.103
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: GBA, Parkinson's disease, genome-wide association, glucocerebrosidase, risk allele
UCL classification: UCL
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 Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases
URI: https://discovery.ucl.ac.uk/id/eprint/10062454
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