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An update on MSA: premotor and non-motor features open a window of opportunities for early diagnosis and intervention. (2020)

First Author: Chelban V

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/10.1007/s00415-020-09881-6

PubMed Identifier: 32436100

Publication URI: http://europepmc.org/abstract/MED/32436100

Type: Journal Article/Review

Volume: 267

Parent Publication: Journal of neurology

Issue: 9

ISSN: 0340-5354