Phenotypic traits and family history in patients with 22q11.2 deletion syndrome and generalized epilepsy: A multicenter case–control study
Emanuele Cerulli Irelli(Sapienza University of Rome), Carlo Di Bonaventura(Sapienza University of Rome), Fabio Di Fabio(Policlinico Umberto I), Thomas Dorn, Agnese Giovannetti(Casa Sollievo della Sofferenza), Flaminia Pugnaloni(Bambino Gesù Children's Hospital), Federica Pulvirenti(Policlinico Umberto I), Antonio Gambardella(Magna Graecia University), Viviana Caputo(Sapienza University of Rome), Antonella Riva(University of Genoa), Georgia Ramantani(University Children's Hospital Zurich), Martine Gavaret(FHU Neurovasc), Carolina Putotto(Sapienza University of Rome), Biagio Orlando(Policlinico Umberto I), Adolfo Mazzeo(Sapienza University of Rome), Gerhard Kluger(Paracelsus Medical University), Tommaso Accinni(Sapienza University of Rome), Cyril Mignot(Sorbonne Université), Francesca Felicia Operto(Magna Graecia University), Anton Iftimovici(Inserm), Cécile Louveau(Inserm), Pasquale Striano(Great Ormond Street Hospital), Martina Fanella(Policlinico Umberto I), Johannes R. Lemke(Leipzig University), Boris Chaumette(Inserm), Edoardo Ferlazzo(Magna Graecia University), Francesco Fortunato(Magna Graecia University)
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