论文信息 - The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa - 字舞流文

The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa

E. Génin | H. Lochmüller | J. Pouget | A. Barois | B. Eymard | C. Desnuelle | D. Grid | P. Richard | B. Chabrol | N. Gouider-Khouja | F. Hentati | S. Bauché | M. Mayer | S. Nouioua | M. Tazir | D. Hantaı̈ | M. Paturneau-Jouas | A. Ammar | A. Hamri | J. Müller | H. Haddad | K. Gaudon | J. Koenig | M. Paturneau‐Jouas