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.
I tiakina i:
| Kaituhi matua: | |
|---|---|
| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
Pediatric Neurology Briefs Publishers
2009-01-01
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| Rangatū: | Pediatric Neurology Briefs |
| Ngā marau: | |
| Urunga tuihono: | https://www.pediatricneurologybriefs.com/articles/233 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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