Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
Haider NB; Jacobson SG; Cideciyan AV; Swiderski R; Streb LM; Searby C; Beck G; Hockey R; Hanna DB; Gorman S; Duhl D; Carmi R; Bennett J; Weleber RG; Fishman GA; Wright AF; Stone EM; Sheffield VC; Nature Genetics, 2000, vol. 24, issue 2, p 127, ISSN 10614036. ISBN 10614036.

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