Behr’s Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene

Pyle A; Ramesh V; Bartsakoulia M; Boczonadi V; Gomez-Duran A; Herczegfalvi, Ágnes; Blakely EL; Smertenko T; Duff J; Moore D; Yu Wai Man P; Douroudis K; Santibanez-Koref M; Griffin H; Lochmüller H; Karcagi V; Taylor RW; Chinnery PF; Horváth, Hilda Rita
Journal article
JOURNAL OF NEUROMUSCULAR DISEASES vol.:1, issue.:1, p.:55-63.
ISSN: 2214-3599
URI: http://repo.lib.semmelweis.hu//handle/123456789/2368
http://dx.doi.org/10.3233/JND-140003
xmlui.dri2xhtml.METS-1.0.item-mtmtid: 2776138
PubMed ID: 26380172
Date: 2014

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