Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate
Neena B. Haider, Samuel G. Jacobson, Artur V. Cideciyan, Ruth E. Swiderski, Luan M. Streb, Charles Searby, Gretel Beck, Robin R. Hockey, David B. Hanna, Susan W. Gorman, David M. Duhl, Rivka Carmi, Jean Bennett, Richard G. Weleber, Gerald A. Fishman, Alan F. Wright, Edwin M. Stone, Val C. Sheffield
Abstract