Charcot-Marie-Tooth Disease Type 1g

Charcot-Marie-Tooth Disease Type 1g, also known as pmp2-related hereditary motor and sensory neuropathy type 1, is related to charcot-marie-tooth disease, demyelinating, type 1g and charcot-marie-tooth disease, x-linked recessive, 2. An important gene associated with Charcot-Marie-Tooth Disease Type 1g is PMP2 (Peripheral Myelin Protein 2), and among its related pathways/superpathways is Intracellular trafficking proteins involved in CMT neuropathy.