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      Demyelinating polyneuropathy in Leber hereditary optic neuropathy.

      1 , , ,
      Neuromuscular disorders : NMD
      Elsevier BV

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          Abstract

          We report a patient with Leber hereditary optic neuropathy (G11778A mtDNA) and a severe demyelinating neuropathy, for which no other cause except his mitochondrial disorder could be found. The involvement of the peripheral nervous system of patients with LHON, in particular with a 11778 mtDNA, is discussed.

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          Author and article information

          Journal
          Neuromuscul. Disord.
          Neuromuscular disorders : NMD
          Elsevier BV
          0960-8966
          0960-8966
          Jun 2006
          : 16
          : 6
          Affiliations
          [1 ] Department of Neurology and Neurophysiology, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands. gilhuis@rdgg.nl
          Article
          S0960-8966(06)00092-7
          10.1016/j.nmd.2006.03.006
          16690316
          6aa83260-679b-462b-a64e-284d43f3522a
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