A Novel Asp121Asn Mutation of Myelin Protein Zero Is Associated with Late-Onset Axonal Charcot-Marie-Tooth Disease, Hearing Loss and Pupil Abnormalities
Xiaohui Duan(Peking University), Dongsheng Fan(King University), Hong Wen(Collaborative Innovation Center of Advanced Microstructures), Shaojie Sun(Qingdao University of Technology), Weihong Gu(China-Japan Friendship Hospital), Renbin Wang(China-Japan Friendship Hospital), Ying Hao(China-Japan Friendship Hospital), Jinsong Jiao(China-Japan Friendship Hospital)
Cited by 9
Related Papers
Stroke in China: advances and challenges in epidemiology, prevention, and management
|The Lancet Neurology|2019|1.6k
Estimated Burden of Stroke in China in 2020
|JAMA Network Open|2023|595
China stroke surveillance report 2021
|Military Medical Research|2023|554
Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing
|Genome Medicine|2019|537
Global variation in prevalence and incidence of amyotrophic lateral sclerosis: a systematic review and meta-analysis
|Journal of Neurology|2019|315