Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate

Neena B. Haider(University of Iowa), Samuel G. Jacobson(University of Pennsylvania), Artur V. Cideciyan(Penn Presbyterian Medical Center), Ruth E. Swiderski(Pediatrics and Genetics), Luan M. Streb(University of Iowa), Charles Searby(Howard Hughes Medical Institute), Gretel Beck(Howard Hughes Medical Institute), Robin R. Hockey(Howard Hughes Medical Institute), David B. Hanna(University of Pennsylvania), Susan W. Gorman, David M. Duhl, Rivka Carmi(Ben-Gurion University of the Negev), Jean Bennett(Penn Presbyterian Medical Center), Richard G. Weleber(Oregon Health & Science University), Gerald A. Fishman(University of Illinois Chicago), Alan F. Wright(Western General Hospital), Edwin M. Stone(University of Iowa), Val C. Sheffield(Pediatrics and Genetics)
Nature Genetics
February 1, 2000
Cited by 506

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