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IOVS.10-5221
IOVS.10-5221
http://dx.doi.org/10.1167/IOVS.10-5221
IQCB1 mutations in patients with leber congenital amaurosis.
P356
Q54408817-6ECEA8E9-E6F2-452F-B14B-4E04E53E5069
P356
IOVS.10-5221
http://dx.doi.org/10.1167/IOVS.10-5221