论文信息 - 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 - 字舞流文

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

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