Publication - 2010 - [O]
• 2010 -
Ben Ammar A, Petit F, Alexandri N, Gaudon K, Bauche S, 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, Hantai D, Richard P, Eymard B:
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7.
J Neurol, 2010, 257 (5):754-766
O
