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. 2013 Nov 5;8(11):e79808. doi: 10.1371/journal.pone.0079808

Figure 1. Family pedigree and skin phenotypes.

Figure 1

(A) Family pedigree. M, mutation; +, normal. An arrow indicates the proband, IV-6. (B) Skin feature of the proband (IV-6) in the family with c.1663C > A. (C) Skin feature of an unrelated patient with sporadic DUH with the c.459 delC mutation.