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. 2016 Jul 20;25(3):111–114. doi: 10.1297/cpe.25.111

Fig. 2.

Fig.
2.

Mutation of NR3C2. The patient, the mother, and two elder brothers each had a heterozygous single base insertion (c.2724insT). This insertion created a premature stop codon (p.Lys909fsX1) in exon 8. In each sequence panel, double bands are present after the insertion site, which is always indicated with an arrow.