Clinical characterization of a novel RAB39B nonstop mutation in a family with ASD and severe ID causing RAB39B downregulation and study of a Rab39b knock down mouse model

por Mignogna, Maria Lidia, Ficarella, Romina, Gelmini, Susanna, Marzulli, Lucia, Ponzi, Emanuela, Gabellone, Alessandra, Peschechera, Antonia, Alessio, Massino, Margari, Lucia, Gentile, Mattia, D’Adamo, Patrizia
Publicado 2021

RAB39B-mediated trafficking of the GluA2-AMPAR subunit controls dendritic spine maturation and intellectual disability-related behaviour

por Mignogna, Maria Lidia, Musardo, Stefano, Ranieri, Giulia, Gelmini, Susanna, Espinosa, Pedro, Marra, Paolo, Belloli, Sara, Murtaj, Valentina, Moresco, Rosa Maria, Bellone, Camilla, D’Adamo, Patrizia
Publicado 2021