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Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
N B Haider, S G Jacobson, A V Cideciyan, R Swiderski, L M Streb, C Searby, G Beck, R Hockey, D B Hanna, S Gorman, D Duhl, R Carmi, J Bennett, R G Weleber, G A Fishman, A F Wright, E M Stone, V C Sheffield
Nat Genet 2000; 24(2):127-131
ICID: 813413
IC™ Value: 50.36
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