Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutations.

Autor:	Dufour, Louis1, Keren, Boris1, Nava, Caroline1,2, Depienne, Christel1,2,3,4, Marzin, Pauline1,5,6, Mignot, Cyril1,5,6, Heron, Delphine1,5,6, Penniello, Marie-José7, Milh, Mathieu8,9, Villard, Laurent8,10, Richelme, Christian11, Rivier, Clotilde12, Whalen, Sandra13, Doummar, Diane5,14,15,16, Lesca, Gaëtan17, Nougues, Marie-Christine14, Dorison, Nathalie14,15, Ville, Dorothée17, Kaminska, Anna17, Panagiotakaki, Eleni17
Zdroj:	Brain & Development. Oct2018, Vol. 40 Issue 9, p768-774. 7p.
Databáze:	Academic Search Ultimate
Externí odkaz:	Zobrazit plný text záznamu Full Text from ScienceDirect