Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate. (Q33888425)
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Current Data About Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
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(P1476) "Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate" (language: en)
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Cideciyan AV
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Swiderski R
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Streb LM
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Beck G
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Hockey R
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Hanna DB
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Gorman S
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Duhl D
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Carmi R
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Bennett J
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Weleber RG
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Fishman GA
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Wright AF
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