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      Multiorgan mitochondrial dysfunction is not a main feature of MFN2 mutations (Reply to: CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder)

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      European Journal of Paediatric Neurology
      Elsevier BV

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          Journal
          European Journal of Paediatric Neurology
          European Journal of Paediatric Neurology
          Elsevier BV
          10903798
          September 2018
          September 2018
          : 22
          : 5
          : 892-893
          Article
          10.1016/j.ejpn.2018.04.011
          2b78c2ff-5f99-435f-92e3-71700ef427cb
          © 2018

          https://www.elsevier.com/tdm/userlicense/1.0/

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