Fig. 2From: Novel SETBP1 mutation in a chinese family with intellectual disabilityResults of Sanger sequencing. The healthy sister (III-5) had a normal gene sequence. The proband (III-9), proband’s sister (III-7), and proband’s mother (II-5) had the same variant (c.942_943insGT, p. Asp316TrpfsTer28) in SETBP1Back to article page