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The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families. (2010)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/awq232

PubMed Identifier: 20819849

Publication URI: http://europepmc.org/abstract/MED/20819849

Type: Journal Article/Review

Volume: 133

Parent Publication: Brain : a journal of neurology

Issue: 10

ISSN: 0006-8950