Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
Neena B. Haider(Massachusetts Eye and Ear Infirmary), Val C. Sheffield(University of Iowa), Charles Searby(Howard Hughes Medical Institute), Richard G. Weleber(Oregon Health & Science University), Robin R. Hockey(Howard Hughes Medical Institute), Artur V. Cideciyan(University of Pennsylvania), Jean Bennett(Penn Presbyterian Medical Center), Susan W. Gorman, Ruth E. Swiderski(Howard Hughes Medical Institute), Samuel G. Jacobson(Penn Presbyterian Medical Center), Edwin M. Stone(Instituto da Visão), David M. Duhl, David B. Hanna(Penn Presbyterian Medical Center), Alan F. Wright(University of Exeter), Gerald A. Fishman(University of Illinois Urbana-Champaign), Luan M. Streb(University of Iowa), Gretel Beck(Howard Hughes Medical Institute), Rivka Carmi(Ben-Gurion University of the Negev)
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