Delineating the neurological phenotype in children with defects in the <scp><i>ECHS1</i></scp> or <scp><i>HIBCH</i></scp> gene
Laura Martí‐Sánchez(Hospital Sant Joan de Déu Barcelona), Belén Pérez‐Dueñas(Vall d'Hebron Hospital Universitari), Roser Pons(National and Kapodistrian University of Athens), Alfons Macaya(Universitat Autònoma de Barcelona), M. Sigatullina(Vall d'Hebron Hospital Universitari), Marta Correa‐Vela(Universitat Autònoma de Barcelona), Anastasia Skouma(Institute of Child Health), Luca Pollini(Sapienza University of Rome), Laura Pérez‐Gay(Hospital Universitario Lucus Augusti), Rosalba Carrozzo(Bambino Gesù Children's Hospital), Ignacio Delgado(Universitat Autònoma de Barcelona), Rafael Artuch(Areté Associates (United States)), Frederic Tort(Instituto de Salud Carlos III), A. Arranz(Vall d'Hebron Hospital Universitari), Vincenzo Leuzzi(Sapienza University of Rome), Luis González‐Gutiérrez‐Solana(Instituto de Salud Carlos III), María Eugenia Yoldi(Navarrabiomed), Roser Urreizti(Red de Investigación en Actividades Preventivas y Promoción de la Salud), Ángel Sánchez‐Montáñez(Vall d'Hebron Hospital Universitari), Serena Galosi(Université de Montpellier), Anna Marcé‐Grau(Universitat Autònoma de Barcelona), Luis Aldámiz‐Echevarría(Hospital de Cruces), Juan Darío Ortigoza‐Escobar(Instituto de Salud Carlos III), Cristiano Rizzo(Cluster in Biomedicine), Eduardo López‐Laso(Hospital Universitario Reina Sofía), Manuela Tolve(Sapienza University of Rome), Antònia Ribes(Instituto de Salud Carlos III), Mireia del Toro(Universitat Autònoma de Barcelona), Filip Roelens(AZ Delta), Diego Martinelli(Bambino Gesù Children's Hospital), Carlo Dionisi‐Vici(Bambino Gesù Children's Hospital), Heidy Baide‐Mairena(Universitat Autònoma de Barcelona), Michela Semeraro(Bambino Gesù Children's Hospital), Élida Vázquez(Vall d'Hebron Hospital Universitari), Sergio Aguilera
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