A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathy
European journal of medical genetics, 2017-06, Vol.60 (6), p.345 [Peer Reviewed Journal]Copyright © 2017 Elsevier Masson SAS. All rights reserved. ;EISSN: 1878-0849 ;DOI: 10.1016/j.ejmg.2017.04.006 ;PMID: 28412374
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