Case report: A novel variant (H49N) in Myelin Protein Zero gene is responsible for a patient with Charcot–Marie–Tooth disease

New Research: Case report: A novel variant (H49N) in Myelin Protein Zero gene is responsible for a patient with Charcot–Marie–Tooth disease: This report presents a case of Charcot–Marie–Tooth dominant intermediate D (CMTDID), a rare subtype of… https://t.c