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Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14 (2018)

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/10.1002/mds.27334

PubMed Identifier: 29603387

Publication URI: http://europepmc.org/abstract/MED/29603387

Type: Journal Article/Review

Parent Publication: Movement Disorders

Issue: 7

ISSN: 0885-3185