Zhonghua nei ke za zhiFemaleHumansMaleCharcot-Marie-Tooth DiseaseMutation
[Genetic variant analysis in patients with autosomal recessive demyelinating Charcot-Marie-Tooth disease].
B Sun, T J Li, Z H Chen, L Ling, H M Cheng, X S Huang, H F Wang
Published: 202610.3760/cma.j.cn112138-20250917-00552
Abstract
Objective: To analyze the clinical and genetic mutation characteristics of Chinese patients with autosomal recessive demyelinating CMT (AR-CMT1/CMT4). Methods: A total of 244 patients clinically diagnosed with CMT at the Department of Neurology, PLA…
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