Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase
| Auteurs | Bahi-Buisson N, El Sabbagh S, Soufflet C, Escande F, Boddaert N, Valayannopoulos V, Bellane-Chantelot C, Lascelles K, Dulac O, Plouin P, De Lonlay P |
| Revue | |
| Année | 2 008 |
| Institut | I2BM |