DOI:
10.1055/s-00000031
Klinische Monatsblätter für Augenheilkunde
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References
Haider NB, Jacobson SG, Cideciyan AV. et al.
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
Nat Genet 2000;
24: 127-131
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