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Mutations in C12orf65 in patients with encephalomyopathy and a mitochondrial translation defect. (2010)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2010.06.004

PubMed Identifier: 20598281

Publication URI: http://europepmc.org/abstract/MED/20598281

Type: Journal Article/Review

Volume: 87

Parent Publication: American journal of human genetics

Issue: 1

ISSN: 0002-9297