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Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatment. (2013)

First Author: Bettencourt C

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/s00415-013-7044-6

PubMed Identifier: 23881105

Publication URI: http://europepmc.org/abstract/MED/23881105

Type: Journal Article/Review

Volume: 260

Parent Publication: Journal of neurology

Issue: 9

ISSN: 0340-5354