CAPRIN1 haploinsufficiency causes an autosomal dominant neurodevelopmental disorder with defects in hiPSCs-derived neurons and an identifiable episignature in patients Lisa Pavinato , Andrea Delle Vedove , Diana Carli , Marta Ferrero , Silvia Carestiato , Jennifer Howe , Emanuele Agolini , Domenico Coviello , Ingrid M. B. H. van de Laar , P. Y. Billie Au , Eleonora Di Gregorio , Alessandra Fabbiani , Susanna Croci , Maria Antonietta Mencarelli , Lucia Bruno , Alessandra Renieri , Danai Veltra , Christalena Sofocleous , Laurence Faivre , Benoit Mazel , Hana Safraou , Anne-Sophie Denomme-Pichon , Marjon van Slegtenhorst , Noor Giesbertz , Richard van Jaarsveld , Anna Childers , Curtis C. Rogers , Antonio Novelli , Silvia De Rubeis , Joseph Buxbaum , Slavica Trajkova , Sadegheh Haghshenas , Haley McConkey , Jennifer Kerkhof , Bekim Sadikovic , Stephen Scherer , Giovanni Battista Ferrero , Brunhilde Wirth , Alfredo Brusco EUROPEAN JOURNAL OF HUMAN GENETICS(2023)
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