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.

Bibliographic Details
Main Author: J Gordon Millichap
Format: Article
Published: Pediatric Neurology Briefs Publishers 2009-01-01
Series:Pediatric Neurology Briefs
Online Access: