A novel founder SCN4A mutation causes painful cold-induced myotonia in French-Canadians
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical)
Cited by 18 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. Targeted Therapies for Skeletal Muscle Ion Channelopathies: Systematic Review and Steps Towards Precision Medicine;Journal of Neuromuscular Diseases;2021-05-13
2. Sodium Channel Myotonia and a Novel Gly701Asp Mutation in the SCN4A Gene: From an Ophthalmological Symptom to a Familial Disease;Neuro-Ophthalmology;2020-07-24
3. Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4;Frontiers in Neurology;2020-04-29
4. Pain in SCN4A Mutated P.A1156T muscle sodium channelopathy-a postal survey;Muscle & Nerve;2018-01-11
5. Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A gene;Neurology;2017-03-22
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