The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa.
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| Description | scientific article |
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author: Hanns Lochmüller Emmanuelle Génin Stéphanie Bauché Pascale Richard |
| Publication date | December 1, 2008 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |