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

dc.contributor.author	Pyle A
dc.contributor.author	Ramesh V
dc.contributor.author	Bartsakoulia M
dc.contributor.author	Boczonadi V
dc.contributor.author	Gomez-Duran A
dc.contributor.author	Herczegfalvi, Ágnes
dc.contributor.author	Blakely EL
dc.contributor.author	Smertenko T
dc.contributor.author	Duff J
dc.contributor.author	Moore D
dc.contributor.author	Yu Wai Man P
dc.contributor.author	Douroudis K
dc.contributor.author	Santibanez-Koref M
dc.contributor.author	Griffin H
dc.contributor.author	Lochmüller H
dc.contributor.author	Karcagi V
dc.contributor.author	Taylor RW
dc.contributor.author	Chinnery PF
dc.contributor.author	Horváth, Hilda Rita
dc.date.accessioned	2017-06-08T08:49:35Z
dc.date.available	2017-06-08T08:49:35Z
dc.date.issued	2014
dc.identifier.citation	pagination=55-63; journalVolume=1; journalIssueNumber=1; journalTitle=JOURNAL OF NEUROMUSCULAR DISEASES;
dc.identifier.uri	http://repo.lib.semmelweis.hu//handle/123456789/2368
dc.identifier.uri	doi:10.3233/JND-140003
dc.relation.ispartof	urn:issn:2214-3599
dc.title	Behr’s Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene
dc.type	Journal Article
dc.date.updated	2015-11-18T08:02:01Z
dc.language.rfc3066	en
dc.identifier.mtmt	2776138
dc.identifier.pubmed	26380172
dc.contributor.department	SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution	Semmelweis Egyetem