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Reply: DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions
Brain ( IF 14.5 ) Pub Date : 2017-12-08 , DOI: 10.1093/brain/awx302 Dario Ronchi , Daniela Piga , Stefano Lamberti , Monica Sciacco , Stefania Corti , Maurizio Moggio , Nereo Bresolin , Giacomo Pietro Comi
Brain ( IF 14.5 ) Pub Date : 2017-12-08 , DOI: 10.1093/brain/awx302 Dario Ronchi , Daniela Piga , Stefano Lamberti , Monica Sciacco , Stefania Corti , Maurizio Moggio , Nereo Bresolin , Giacomo Pietro Comi
Sir,
中文翻译：
回复：CPEO，线粒体肌病，帕金森病和mtDNA缺失患者的DGUOK隐性突变
先生，
更新日期：2017-12-08
中文翻译：
回复：CPEO，线粒体肌病，帕金森病和mtDNA缺失患者的DGUOK隐性突变
先生，
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