Publication | Closed Access

De novo mutation of the myelin Po gene in Dejerine–Sottas disease (hereditary motor and sensory neuropathy type III)

Hereditary MotorNeurobiology Of DiseaseDejerine–sottas DiseaseNeurological DisorderMedicineNeuromotor DisordersGeneticsGenetic DisorderMyelin Po GeneDegenerative DiseaseMotor DisorderNeurologyNeuroscienceNeuropathologyNeuromuscular PathologySocial SciencesNeurogenetics