A new mouse model for the slow-channel congenital myasthenic syndrome induced by the AChR εL221F mutation
Author:
Publisher
Elsevier BV
Subject
Neurology
Reference35 articles.
1. Reduced acetylcholine receptor density, morphological remodeling, and butyrylcholinesterase activity can sustain muscle function in acetylcholinesterase knockout mice;Adler;Muscle Nerve,2004
2. Hereditary myasthenic syndromes with late onset. Value of electrophysiological tests;Chauplannaz;Rev. Neurol. (Paris),1994
3. A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions;Chevessier;Hum. Mol. Genet.,2008
4. Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes;Croxen;Neurology,2002
5. Decremental response to high-frequency trains of acetylcholine pulses but unaltered fractional Ca2+ in a panel of “slow-channel syndrome” nicotinic receptor mutants;Elenes;J. Gen. Physiol.,2009
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