| Title : The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa - Richard_2008_Neurology_71_1967 |
| Author(s) : Richard P , Gaudon K , Haddad H , Ammar AB , Genin E , Bauche S , Paturneau-Jouas M , Muller JS , 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 |
| Ref : Neurology , 71 :1967 , 2008 |
| Abstract : Richard_2008_Neurology_71_1967 |
| ESTHER : Richard_2008_Neurology_71_1967 |
| PubMedSearch : Richard_2008_Neurology_71_1967 |
| PubMedID: 19064877 |
Richard P, Gaudon K, Haddad H, Ammar AB, Genin E, Bauche S, Paturneau-Jouas M, Muller JS, 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 (2008)
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
Neurology
71 :1967
Richard P, Gaudon K, Haddad H, Ammar AB, Genin E, Bauche S, Paturneau-Jouas M, Muller JS, 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 (2008)
Neurology
71 :1967