CHRNE Mutation and Congenital Myasthenia
DOI:
https://doi.org/10.15844/pedneurbriefs-23-1-8Keywords:
Oculobulbar Involvement, Mild and Stable Course, Cholinesterase InhibitorsAbstract
The CHRNE e1293insG mutation was identified in 14 (60%) of 23 North African families with an early onset form of congenital myasthenic syndrome studied at centers in France, Tunisia, Algeria, and UK.Published
2009-01-01
Issue
Section
Neuromuscular Disorders
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