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. 2016 Sep 19;7(9):65. doi: 10.3390/genes7090065

Figure 1.

Figure 1

Pedigree and mutations of families 1–7. Families 1–5 harbored Ectodysplasin A (EDA) mutations: c.662G>A (p.Gly221Asp), c.741G>A (p.Gln247Gln), c.463C>T (p.Arg155Cys), c.1013C>T (p.Thr338Met) and c.895G>A (p.Gly299Ser). In family 6, Ectodysplasin A receptor (EDAR) mutation c.1259G>A (p.Arg420Gln) was identified. WNT10A mutation c.354T>G (p.Tyr118*) and c.637G>A (p.Gly213Ser) were identified in family 7. Black arrows point to the probands. Red arrows point to the mutations. “+” indicates that the blood sample is available for genetic analysis in this study. In family 1, the sequence chromatogram showed reverse complemented sequence. The remaining sequence chromatograms showed forward sequence.