Lysosomal storage disorder gene variants in multiple system atrophy
Brain
.
2018 Jul 1;141(7):e53.
doi: 10.1093/brain/awy124.
Authors
Lasse Pihlstrøm
1
2
3
,
Lucia Schottlaender
1
2
4
,
Viorica Chelban
1
2
5
;
MSA Exome Consortium
;
Wassilios G Meissner
6
,
Monica Federoff
7
,
Andy Singleton
7
,
Henry Houlden
1
2
Affiliations
1
Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK.
2
National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.
3
Oslo University Hospital, Oslo, Norway.
4
Dubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London, UK.
5
Department of Neurology and Neurosurgery, Institute of Emergency Medicine, Chisinau, Republic of Moldova.
6
Department of Neurology, University Hospital Bordeaux, France.
7
Laboratory of Neurogenetics, NIH/NIA, Bethesda, USA.
PMID:
29741613
PMCID:
PMC6057515
DOI:
10.1093/brain/awy124
No abstract available
Publication types
Letter
Research Support, Non-U.S. Gov't
Comment
MeSH terms
Humans
Lysosomal Storage Diseases*
Multiple System Atrophy*
Parkinson Disease*
Grants and funding
104033/WT_/Wellcome Trust/United Kingdom
MR/J004758/1/MRC_/Medical Research Council/United Kingdom
WT_/Wellcome Trust/United Kingdom
G0802760/MRC_/Medical Research Council/United Kingdom
G1001253/MRC_/Medical Research Council/United Kingdom