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IOVS.18-24817
IOVS.18-24817
http://dx.doi.org/10.1167/IOVS.18-24817
Clinical Characterization of 66 Patients With Congenital Retinal Disease Due to the Deep-Intronic c.2991+1655A>G Mutation in CEP290
P356
Q91332592-86997BDC-53C5-4B34-A1C2-54055BE9FB7E
P356
IOVS.18-24817
http://dx.doi.org/10.1167/IOVS.18-24817