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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| Formato: | Artigo |
| Idioma: | Inglês |
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Pediatric Neurology Briefs Publishers
2009-01-01
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| Series: | Pediatric Neurology Briefs |
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| Acceso en liña: | https://www.pediatricneurologybriefs.com/articles/233 |
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