Reply: DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions

Dario Ronchi; Daniela Piga; Stefano Lamberti; Monica Sciacco; Stefania Corti; Maurizio Moggio; Nereo Bresolin; Giacomo Pietro Comi

doi:10.1093/brain/awx302

Reply: DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions

Dario Ronchi, Daniela Piga, Stefano Lamberti, Monica Sciacco, Stefania Corti, Maurizio Moggio, Nereo Bresolin, Giacomo Pietro Comi

Fondazione IRCCS Ca' Granda- Ospedale Maggiore Policlinico

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	e4
Journal	Brain
Volume	141
Issue number	1
DOIs	https://doi.org/10.1093/brain/awx302
Publication status	Published - Jan 1 2018

ASJC Scopus subject areas

Clinical Neurology

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10.1093/brain/awx302

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author = "Dario Ronchi and Daniela Piga and Stefano Lamberti and Monica Sciacco and Stefania Corti and Maurizio Moggio and Nereo Bresolin and {Pietro Comi}, Giacomo",

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AU - Piga, Daniela

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AU - Sciacco, Monica

AU - Corti, Stefania

AU - Moggio, Maurizio

AU - Bresolin, Nereo

AU - Pietro Comi, Giacomo

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Reply: DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions

ASJC Scopus subject areas

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