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      A French family with Charcot–Marie–Tooth disease related to simultaneous heterozygous MFN2 and GDAP1 mutations

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      Journal: Neuromuscular Disorders
      Publisher: Elsevier BV

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          DOI:: 10.1016/j.nmd.2012.04.001
          PubMed ID:: 22546700
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          https://www.elsevier.com/tdm/userlicense/1.0/

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