Lysosomal storage disorder gene variants in multiple system atrophy

Lasse Pihlstrøm, Lucia Schottlaender, Viorica Chelban, Wassilios G Meissner, Monica Federoff, Andy Singleton, Henry Houlden,
Brain. 2018-05-07; 141(7): e53-e53
DOI: 10.1093/brain/awy124


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1. Brain. 2018 Jul 1;141(7):e53. doi: 10.1093/brain/awy124.

Lysosomal storage disorder gene variants in multiple system atrophy.

Pihlstrøm L(1)(2)(3), Schottlaender L(1)(2)(4), Chelban V(1)(2)(5); MSA Exome
Consortium, Meissner WG(6), Federoff M(7), Singleton A(7), Houlden H(1)(2).

Author information:
(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.

DOI: 10.1093/brain/awy124
PMCID: PMC6057515 [Available on 2019-07-01]
PMID: 29741613

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