1. Netrin‐G2 dysfunction causes a Rett‐like phenotype with areflexia. Issue 2 (15th November 2019) Authors: Heimer, Gali; van Woerden, Geeske M.; Barel, Ortal; Marek‐Yagel, Dina; Kol, Nitzan; Munting, Johannes B.; Borghei, Minoeshka; Atawneh, Osama M.; Nissenkorn, Andreea; Rechavi, Gideon; Anikster, Yair; Elgersma, Ype; Kushner, Steven A.; Ben Zeev, Bruria Journal: Human mutation Issue: Volume 41:Issue 2(2020) Page Start: 476 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗