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Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophy. (2014)

First Author: Tucci 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/10.1136/jnnp-2013-306387

PubMed Identifier: 24198383

Publication URI: http://europepmc.org/abstract/MED/24198383

Type: Journal Article/Review

Volume: 85

Parent Publication: Journal of neurology, neurosurgery, and psychiatry

Issue: 5

ISSN: 0022-3050