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. 2023 Apr 12;2023(2):22-0362. doi: 10.1530/EDM-22-0362

Figure 2.

Figure 2

Sequencing results of genomic DNA (A–D) and cDNA (E, F) of the insulin receptor gene (INSR). The proband, his mother, and his grandfather have a heterozygous GTG deletion at the 3′ end of exon 17. Sequencing of genomic DNA could not distinguish between this mutation and a GTG deletion next to it at the 5′ end of the intron. Sequencing of cDNA confirmed the mutation as p.Val1086del in exon 17.