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Absence of HINT1 mutations in a UK and Spanish cohort of patients with inherited neuropathies. (2015)

First Author: Horga A

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/s00415-015-7851-z

PubMed Identifier: 26194197

Publication URI: http://europepmc.org/abstract/MED/26194197

Type: Journal Article/Review

Volume: 262

Parent Publication: Journal of neurology

Issue: 8

ISSN: 0340-5354