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.
Date
01-01-2009
Author
J Gordon Millichap
Metadata
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URI
https://www.pediatricneurologybriefs.com/articles/233
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