Charcot-Marie-Tooth Disease, Demyelinating, Type 4f (CMT4F)

Charcot-Marie-Tooth Disease, Demyelinating, Type 4f, also known as charcot-marie-tooth disease type 4f, is related to hereditary neuropathies and hereditary sensory neuropathy, and has symptoms including ataxia, sensory An important gene associated with Charcot-Marie-Tooth Disease, Demyelinating, Type 4f is PRX (Periaxin), and among its related pathways/superpathways are PI Metabolism and Intracellular trafficking proteins involved in CMT neuropathy. Affiliated tissues include skeletal muscle and spinal cord, and related phenotypes are vocal cord paresis and scoliosis