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Heterogeneity in clinical features and disease severity in ataxia-associated SYNE1 mutations. (2016)

First Author: Wiethoff S

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/s00415-016-8148-6

PubMed Identifier: 27178001

Publication URI: http://europepmc.org/abstract/MED/27178001

Type: Journal Article/Review

Volume: 263

Parent Publication: Journal of neurology

Issue: 8

ISSN: 0340-5354