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Loss-of-function variants in CAPRIN1 in patients affected by autism spectrum disorder, language delay and intellectual disability with variable expressivity and incomplete penetrance

Title: Loss-of-function variants in CAPRIN1 in patients affected by autism spectrum disorder, language delay and intellectual disability with variable expressivity and incomplete penetrance
Authors: Pavinato, L; Howe, JL; Carli, D; Agolini, E; Coviello, DA; Van de Laar, IMBH; Au, PYB; Di Gregorio, E; Giorgio, E; Pozzi, E; Ferrero, M; Cardaropoli, S; Delle Vedove, A; Salpietro, V; Zara, F; Novelli, A; Wirth, B; Ferrero, GB; Scherer, SW; Brusco, A
Contributors: Pavinato, L; Howe, JL; Carli, D; Agolini, E; Coviello, DA; Van de Laar, IMBH; Au, PYB; Di Gregorio, E; Giorgio, E; Pozzi, E; Ferrero, M; Cardaropoli, S; Delle Vedove, A; Salpietro, V; Zara, F; Novelli, A; Wirth, B; Ferrero, GB; Scherer, SW; Brusco, A
Publication Year: 2020
Collection: Università degli studi di Torino: AperTo (Archivio Istituzionale ad Accesso Aperto)
Document Type: conference object
Language: English
Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000598482601155; European Human Genetics Virtual Conference 2020; volume:28; issue:SUPPL 1; firstpage:322; lastpage:322; numberofpages:1; journal:EUROPEAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/2318/1796686
Availability: http://hdl.handle.net/2318/1796686
Accession Number: edsbas.98EF2208
Database: BASE