A novel mutation in the TPR6 domain of the RAPSN gene associated with congenital myasthenic syndrome.

Abstract

Congenital myasthenic syndromes (CMS) are rare genetic disorders characterized by impaired neuromuscular transmission. They are caused by mutations in synaptic, presynaptic and post synaptic proteins. Rapsyn is a postsynaptic peripheral membrane protein that anchors the nicotinic acetylcholine receptor to the motor endplate. CMS patients of Iraqi and… (More)
DOI: 10.1016/j.jns.2012.01.012

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