Congenital myasthenic syndrome caused by prolonged acetylcholine receptor channel openings due to a mutation in the M2 domain of the epsilon subunit.

Source:http://linkedlifedata.com/resource/pubmed/id/7531341

Proc. Natl. Acad. Sci. U.S.A. 1995 Jan 31 92 3 758-62

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PMID
7531341