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- W2018502004 abstract "Investigation of congenital myasthenic syndromes (CMSs) disclosed a diverse array of molecular targets at the motor endplate. Clinical, electrophysiologic and morphologic studies paved the way for detecting CMS-related mutations in proteins such as the acetylcholine receptor, acetylcholinesterase, choline acetyltransferase, rapsyn, MuSK and Nav1.4. Analysis of electrophysiologic and biochemical properties of mutant proteins expressed in heterologous systems contributed crucially to defining the molecular consequences of the observed mutations and resulted in improved therapy of different CMSs. Recent crystallography studies of choline acetyltransferase and homology structural models of the acetylcholine receptor are providing further clues to how point mutations alter protein function." @default.
- W2018502004 created "2016-06-24" @default.
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- W2018502004 date "2005-06-01" @default.
- W2018502004 modified "2023-10-04" @default.
- W2018502004 title "Current understanding of congenital myasthenic syndromes" @default.
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- W2018502004 doi "https://doi.org/10.1016/j.coph.2004.12.007" @default.
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