The phenotype of severe early childhood onset retinal dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosis

Richard G. Weleber, Michel Michaelides, Karmen M. Trzupek, Niamh B. Stover, Edwin M. Stone

Research output: Contribution to journal › Article › peer-review

61 Scopus citations

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Medicine & Life Sciences