Slow-Channel Myasthenic Syndrome Caused By Enhanced Activation, Desensitization, and Agonist Binding Affinity Attributable to Mutation in the M2 Domain of the Acetylcholine Receptor α Subunit-Reference-Cited by-同舟云学术

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Slow-Channel Myasthenic Syndrome Caused By Enhanced Activation, Desensitization, and Agonist Binding Affinity Attributable to Mutation in the M2 Domain of the Acetylcholine Receptor α Subunit

Published:1997-08-01 Issue:15 Volume:17 Page:5651-5665
ISSN:0270-6474
Container-title:The Journal of Neuroscience
language:en
Short-container-title:J. Neurosci.

Author:

Milone Margherita,Wang Hai-Long,Ohno Kinji,Fukudome Takayasu,Pruitt J. Ned,Bren Nina,Sine Steven M.,Engel Andrew G.

Publisher

Society for Neuroscience

Subject

General Neuroscience

Cited by 112 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. Pathogenic residue insertion in neuronal nicotinic receptor alters intra- and inter-subunit interactions that tune channel gating;Journal of Biological Chemistry;2024-05

2. Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes—A Comprehensive Review;International Journal of Molecular Sciences;2023-02-13

3. Slow Channel Syndrome Revisited: 40 Years Clinical Follow-Up and Genetic Characterization of Two Cases;Journal of Neuromuscular Diseases;2022-07-01

4. Diagnosis of DOK7 congenital myasthenic syndrome during pregnancy: A case report and literature review;Clinical Neurology and Neurosurgery;2021-04

5. Slow-Channel Congenital Myasthenic Syndrome due to a Novel Mutation in the Acetylcholine Receptor Alpha Subunit in a South Asian: A Case Report;Journal of Neuromuscular Diseases;2021-01-01

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