Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorder - 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; Syrbe, Steffen (Human mutation, 2021)
Gesehen am 15.08.2023