Diverse molecular mechanisms involved in AChR deficiency due to rapsyn mutations
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/129/10/2773/824978/awl219.pdf
Cited by 48 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. Dystrophic Myopathy of the Diaphragm with Recurrent Severe Respiratory Failure is Congenital Myasthenic Syndrome 11;Journal of Neuromuscular Diseases;2023-03-07
2. The role of Rapsyn in neuromuscular junction and congenital myasthenic syndrome;Biomolecules and Biomedicine;2023-02-20
3. Clinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes—A Comprehensive Review;International Journal of Molecular Sciences;2023-02-13
4. Neurogenetic motor disorders;Motor System Disorders, Part I: Normal Physiology and Function and Neuromuscular Disorders;2023
5. Membraneless condensates by Rapsn phase separation as a platform for neuromuscular junction formation;Neuron;2021-06
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