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Lysosomal storage disorder gene variants in multiple system atrophy. (2018)

First Author: Pihlstrøm L

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awy124

PubMed Identifier: 29741613

Publication URI: http://europepmc.org/abstract/MED/29741613

Type: Journal Article/Review

Volume: 141

Parent Publication: Brain : a journal of neurology

Issue: 7

ISSN: 0006-8950