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Autor:
Emmanuel Raffo, Mathilde Lefebvre, Agathe Roubertie, Mondher Chouchane, Yannis Duffourd, Nathalie Villeneuve, Sandra Wahlen, Arnaud Lafon, Gaetan Lesca, Anne de Saint Martin, Delphine Héron, Laurent Villard, Cyril Mignot, Mathieu Milh, Alice Masurel-Paulet, Sylvie Odent, Laurence Faivre, Salima El Chehadeh, Annick Toutain, Julien Thevenon, Christel Thauvin-Robinet, Frédéric Huet, Bertrand Isidor, Clara Jugé, Jean-Baptiste Rivière, Christophe Philippe, Judith St-Onge, Damien Sanlaville, Véronique Darmency-Stamboul, François Feillet
Publikováno v:
American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), 2014, 95 (1), pp.113-120. 〈10.1016/j.ajhg.2014.06.006〉
American Journal of Human Genetics, 2014, 95 (1), pp.113-120. ⟨10.1016/j.ajhg.2014.06.006⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2014, 95 (1), pp.113-120. ⟨10.1016/j.ajhg.2014.06.006⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2014, 95 (1), pp.113-120. 〈10.1016/j.ajhg.2014.06.006〉
American Journal of Human Genetics, 2014, 95 (1), pp.113-120. ⟨10.1016/j.ajhg.2014.06.006⟩
American Journal of Human Genetics, Elsevier (Cell Press), 2014, 95 (1), pp.113-120. ⟨10.1016/j.ajhg.2014.06.006⟩
International audience; Epileptic encephalopathy (EE) refers to a clinically and genetically heterogeneous group of severe disorders characterized by seizures, abnormal interictal electro-encephalogram, psychomotor delay, and/or cognitive deteriorati