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RCBTB1 Mutations Identified in Six Families Affected by Syndromic and Non-syndromic iRD
Filled symbols represent affected individuals, whereas clear symbols represent unaffected individuals. A double line represents reported consanguinity. Genotypes of different family members are indicated below them. Individuals who underwent identity-by-descent mapping and/or whole-exome sequencing are indicated by IBD and WES, respectively.
