1. Recurrent homozygous damaging mutation in TMX2, encoding a protein disulfide isomerase, in four families with microlissencephaly. Issue 4 (5th October 2019) Authors: Ghosh, Shereen Georges; Wang, Lu; Breuss, Martin W; Green, Joshua D; Stanley, Valentina; Yang, Xiaoxu; Ross, Danica; Traynor, Bryan J; Alhashem, Amal M; Azam, Matloob; Selim, Laila; Bastaki, Laila; Elbastawisy, Hanan I; Temtamy, Samia; Zaki, Maha; Gleeson, Joseph G Journal: Journal of medical genetics Issue: Volume 57:Issue 4(2020) Page Start: 274 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗