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 Swiderski, Luan M. Streb, Charles Searby, Gretel Beck, Robin Hockey, David B. Hanna, Susan Gorman, David Duhl, Rivka Carmi, Jean Bennett, Richard G. Weleber, Gerald A. Fishman, Alan F. Wright, Edwin M. Stone, Val C. Sheffield

Research output: Contribution to journal › Article › peer-review