<i>GABBR2</i> mutations determine phenotype in rett syndrome and epileptic encephalopathy
Yongjin Yoo(Korea University), Murim Choi(Seoul National University), Jinhong Wie(Catholic University of Korea), JeaYeok Hong(Yonsei University), Ki Joong Kim(Seoul National University Hospital), Youngha Lee(Seoul National University), Christopher Castaldi(Yale University), Natasha Shur(Albany Medical Center Hospital), Roseànne S. Ebel(Center for Human Genetics), Je‐Sang Lee(Gachon University Gil Medical Center), Chansik Hong(Chosun University), Shrikant Mane(Yale Cancer Center), Kaya Bilgüvar(Yale Cancer Center), Jae Young Seong(Korea University), Jong‐Hee Chae(Seoul National University), Lindsay B. Henderson(Johns Hopkins University), Cheryl Clow(Albany Medical Center Hospital), Jane Jung(Yonsei University), Rebecca Willaert, Seok‐Geun Lee(Kyung Hee Cyber University), Eunjung Na(Yonsei University), Jin Sook Lee(Gachon University Gil Medical Center), Sang‐Yoon Park(Hallym University), Insuk So(Seoul National University), Yong Beom Shin(Pusan National University Hospital), Hosung Jung(Yonsei University), Byung Chan Lim(Seoul National University Children's Hospital), Hyosuk Cho(Seoul National University), Hee‐Jung Choi(Seoul National University), Kathryn Miller(Albany Medical Center Hospital), Yong Seung Hwang(Seoul National University Children's Hospital), Eunjin Kim(Yonsei University), Yoo‐Na Lee(Seoul National University), Suzanne D. DeBrosse(Center for Human Genetics), Irina Tikhonova(Yale University)
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