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NDUFA4 mutations underlie dysfunction of a cytochrome c oxidase subunit linked to human neurological disease. (2013)

First Author: Pitceathly RD

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/10.1016/j.celrep.2013.05.005

PubMed Identifier: 23746447

Publication URI: http://europepmc.org/abstract/MED/23746447

Type: Journal Article/Review

Volume: 3

Parent Publication: Cell reports

Issue: 6