Published 2009
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CHRNE Mutation and Congenital Myasthenia
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Abstract
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.Files
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- PNB-23-07-a
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2009When the item was originally created.