1. 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. Issue 9 (11th November 2021) Authors: Mignogna, Maria Lidia; Ficarella, Romina; Gelmini, Susanna; Marzulli, Lucia; Ponzi, Emanuela; Gabellone, Alessandra; Peschechera, Antonia; Alessio, Massino; Margari, Lucia; Gentile, Mattia; D'Adamo, Patrizia Journal: Human molecular genetics Issue: Volume 31:Issue 9(2022) Page Start: 1389 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗