HAL Id: hal-01817830
https://hal.umontpellier.fr/hal-01817830
Submitted on 20 Mar 2020
HAL is a multi-disciplinary open access
archive for the deposit and dissemination of sci-entific research documents, whether they are pub-lished or not. The documents may come from teaching and research institutions in France or abroad, or from public or private research centers.
L’archive ouverte pluridisciplinaire HAL, est destinée au dépôt et à la diffusion de documents scientifiques de niveau recherche, publiés ou non, émanant des établissements d’enseignement et de recherche français ou étrangers, des laboratoires publics ou privés.
A recessive Na v 1.4 mutation underlies congenital
myasthenic syndrome with periodic paralysis
Karima Habbout, Hugo Poulin, Francois Rivier, Serena Giuliano, Damien
Sternberg, Bertrand Fontaine, Bruno Eymard, Raul Juntas Morales, Bernard
Echenne, Louise King, et al.
To cite this version:
Karima Habbout, Hugo Poulin, Francois Rivier, Serena Giuliano, Damien Sternberg, et al.. A recessive Na v 1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. Neurology, American Academy of Neurology, 2016, 86 (2), pp.161-169. �10.1212/WNL.0000000000002264�. �hal-01817830�