Novel MFN2 Missense Mutation Induces Hereditary Axonal Motor and Sensory Neuropathy in a Saudi Arabian Family.
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DOI: 10.1097/cnd.0000000000000244
Abstract: Hereditary axonal motor and sensory neuropathy or Charcot-Marie-Tooth type 2 (CMT2) is a common inherited peripheral neuropathy. Major symptomatologic signs vary from minimal to significant weakness and loss of sensation, feet usually affected more than… read more here.
Keywords: sensory neuropathy; saudi arabian; axonal motor; motor sensory ... See more keywords