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ARCHOPHT.122.7.1029
ARCHOPHT.122.7.1029
http://dx.doi.org/10.1001/ARCHOPHT.122.7.1029
The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations.
P356
Q34332943-07FAD10A-1298-41AD-A9C3-B6566D3B7A35
P356
ARCHOPHT.122.7.1029
http://dx.doi.org/10.1001/ARCHOPHT.122.7.1029