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
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R. Ficarella | Emanuela Ponzi | P. D’Adamo | M. Gentile | L. Margari | M. Mignogna | A. Gabellone | L. Marzulli | Antonia Peschechera | Susanna Gelmini | Massino Alessio