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      G.P.3.05 A novel heteroplasmic mitochondrial MT-ND5 frameshift mutation causing isolated paediatric complex I deficiency

      , , , ,
      Neuromuscular Disorders
      Elsevier BV

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          Journal
          Neuromuscular Disorders
          Neuromuscular Disorders
          Elsevier BV
          09608966
          September 2009
          September 2009
          : 19
          : 8-9
          : 562-563
          Article
          10.1016/j.nmd.2009.06.063
          dec4b286-bac0-4c74-a7cf-5a5aff8da2f2
          © 2009

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

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