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. 2012 Sep 18;158A(11):2788–2796. doi: 10.1002/ajmg.a.35583

FIG. 5.

FIG. 5

Sequence chromatograms of exon 3 of the IER3IP1 gene showing the point mutation c.T233C detected as homozygous in the affected patients from each family, heterozygous in both parents, and homozygous wildtype in both unaffected siblings.