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Four novel connexin 32 mutations in X-linked Charcot-Marie-Tooth disease. Phenotypic variability and central nervous

Georgia Karadima1, Georgios Koutsis1, Maria Raftopoulou1

  • 1Neurogenetics Unit, 1st Department of Neurology, University of Athens Medical School, Eginition Hospital, Athens, Greece.

Journal of the Neurological Sciences
|April 29, 2014
PubMed

Keywords:
CMTXCNS involvementCharcot- Marie- ToothConnexin 32GJB1Mutation

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