Media type: E-Article Title: Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder Contributor: Semino, Francesca; Schröter, Julian; Willemsen, Marjolein H.; Bast, Thomas; Biskup, Saskia; Beck‐Woedl, Stefanie; Brennenstuhl, Heiko; Schaaf, Christian P.; Kölker, Stefan; Hoffmann, Georg F.; Haack, Tobias B.; Syrbe, Steffen imprint: Hindawi Limited, 2021 Published in: Human Mutation Language: English DOI: 10.1002/humu.24245 ISSN: 1098-1004; 1059-7794 Origination: Footnote: