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. 2024 Dec 16;25(24):13471. doi: 10.3390/ijms252413471

Figure 1.

Figure 1

Pedigree of the extended family. Black-filled boxes represent affected individuals with a clinical presentation suggestive of a defect in the NER pathway and carry homozygous variants in both ERCC4 and OTOA. The parents (III−1 and III−2) are healthy individuals heterozygous for both the ERCC4 and OTOA variants.