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. 2016 Dec 14;102(3):942–949. doi: 10.1210/jc.2016-3164

Figure 2.

Figure 2.

Pedigrees of 5 children with HI associated with mutations in UCP2. Arrows indicate probands diagnosed with HI. DNA was unavailable for testing in individuals without a number. ▪,●, hypoglycemia diagnosed; ⋄, multiple individuals not tested. *Case 3 also carried a paternally inherited novel variant of unknown significance in HNF1A (p.Gly574Asp) (see text). wt, wild-type.