The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa - Vigipallia

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The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa

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Richard, P. | Gaudon, K. | Haddad, H. | Ammar, A. | Genin, E. | Bauché, Stéphanie | Paturneau-Jouas, M. | Muller, J. | Lochmuller, H. | Grid, D. | Hamri, A. | Nouioua, S. | Tazir, M. | Mayer, M. | Desnuelle, C. | Barois, A. | Chabrol, B. | Pouget, J. | Koenig, J. | Gouider-Khouja, N. | Hentati, F. | Eymard, B. | Hantai, D.

Edité par CCSD ; American Academy of Neurology -

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Langue: en

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