New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/5/9/1217/1657649/5-9-1217.pdf
Cited by 182 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. The effect of unliganded gating on agonist response in nicotinic receptors;European Journal of Pharmacology;2024-10
2. Structural switch in acetylcholine receptors in developing muscle;Nature;2024-07-31
3. Congenital myasthenic syndromes;Handbook of Clinical Neurology;2024
4. Mechanism of hydrophobic gating in the acetylcholine receptor channel pore;Journal of General Physiology;2023-12-28
5. Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes—A Comprehensive Review;International Journal of Molecular Sciences;2023-02-13
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