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. Author manuscript; available in PMC: 2021 Jun 29.
Published in final edited form as: Eur J Dermatol. 2018 Apr 1;28(2):209–216. doi: 10.1684/ejd.2017.3210

Figure 2.

Figure 2.

Sequence analysis of the ST14 gene revealing the mutation c.1315G>A (p.Gly439Ser). Upper panel (A) represents the nucleotide sequence of an affected individual, middle panel (B) a heterozygous carrier, and lower panel (C) a homozygous normal individual. The arrow indicates the missense mutation.