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Mov Disord. 2018 Nov;33(11):1821-1823. doi: 10.1002/mds.103. Epub 2018 Oct 9.

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

Author information

1
Laboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA.
2
UK Dementia Research Institute at UCL and Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, UK.
3
Founder/consultant with Data Tecnica International, Glen Echo, Maryland, USA.
4
School of Pharmacy, University of Reading, Reading, UK.
5
Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London, UK.

KEYWORDS:

GBA; Parkinson's disease; genome-wide association; glucocerebrosidase; risk allele

PMID:
30302829
PMCID:
PMC6379910
DOI:
10.1002/mds.103
[Indexed for MEDLINE]
Free PMC Article

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