CHRNE Mutation and Congenital Myasthenia
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.
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| Format: | Book |
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Pediatric Neurology Briefs Publishers,
2009-01-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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