Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7 - Archive ouverte HAL
Article Dans Une Revue Journal of Neurology Année : 2010

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

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hal-03864208 , version 1 (21-11-2022)

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A. Ben Ammar, F. Petit, N. Alexandri, K. Gaudon, Stéphanie Bauché, et al.. Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7. Journal of Neurology, 2010, 257 (5), pp.754-766. ⟨10.1007/s00415-009-5405-y⟩. ⟨hal-03864208⟩
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