Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7 - Vigipallia

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Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7

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Ben Ammar, A. | Petit, F. | Alexandri, N. | Gaudon, K. | Bauché, Stéphanie | Rouche, A. | Gras, D. | Fournier, E. | Koenig, J. | Stojkovic, T. | Lacour, A. | Petiot, P. | Zagnoli, F. | Viollet, L. | Pellegrini, N. | Orlikowski, D. | Lazaro, L. | Ferrer, X. | Stoltenburg, G. | Paturneau-Jouas, M. | Hentati, F. | Fardeau, M. | Sternberg, D. | Hantaï, D. | Richard, P. | Eymard, B.

Edité par CCSD ; Springer Verlag -

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