Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectively.
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S. Jacobson | M. Othman | D. Vollrath | Yun Li | E. Schwinger | J. Richards | Debra Thompson | C. McHenry | A. Gal | Debra Thompson