1. Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders. Issue 11 (14th August 2017) Authors: Sollis, Elliot; Deriziotis, Pelagia; Saitsu, Hirotomo; Miyake, Noriko; Matsumoto, Naomichi; Hoffer, Mariëtte J.V.; Ruivenkamp, Claudia A.L.; Alders, Mariëlle; Okamoto, Nobuhiko; Bijlsma, Emilia K.; Plomp, Astrid S.; Fisher, Simon E. Journal: Human mutation Issue: Volume 38:Issue 11(2017) Page Start: 1542 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗