A novel mutation of the myelin P0 gene segregating Charcot-Marie-Tooth disease type 1B manifesting as trigeminal nerve thickening
Author:
Publisher
BMJ
Subject
Psychiatry and Mental health,Neurology (clinical),Surgery
Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Prevalence and significance of cranial nerve imaging abnormalities in patients with hereditary neuropathies: Clinical implications at the skull base;Laryngoscope Investigative Otolaryngology;2020-01-10
2. A charcot‐marie‐tooth type 1B kindred associated with hemifacial spasm and trigeminal neuralgia;Muscle & Nerve;2019-04-08
3. The spectrum of Charcot-Marie-Tooth disease due to myelin protein zero: An electrodiagnostic, nerve ultrasound and histological study;Clinical Neurophysiology;2018-01
4. Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder;BMC Medical Genetics;2017-03-23
5. Atypical presentation of Charcot–Marie–Tooth disease 1A: A case report;Neuromuscular Disorders;2015-11
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