1. GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy. Issue 3 (22nd September 2017) Authors: Yoo, Yongjin; Jung, Jane; Lee, Yoo‐Na; Lee, Youngha; Cho, Hyosuk; Na, Eunjung; Hong, JeaYeok; Kim, Eunjin; Lee, Jin Sook; Lee, Je Sang; Hong, Chansik; Park, Sang‐Yoon; Wie, Jinhong; Miller, Kathryn; Shur, Natasha; Clow, Cheryl; Ebel, Roseànne S.; DeBrosse, Suzanne D.; Henderson, Lindsay B.; Willa... Journal: Annals of neurology Issue: Volume 82:Issue 3(2017) Page Start: 466 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗