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518426
518426
http://dx.doi.org/10.1086/518426
Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa
P356
Q24676600-7B2D51B1-C466-4463-8AF8-C6F03A4BCBD4
P356
518426
http://dx.doi.org/10.1086/518426