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. Author manuscript; available in PMC: 2016 May 18.
Published in final edited form as: J Invest Dermatol. 2015 Jul 23;135(12):3192–3194. doi: 10.1038/jid.2015.292

Figure 1. Identification of SASH1S519N in an inherited lentiginosis.

Figure 1

(a) Sequence chromatograms of an unaffected and an affected individual, with a heterozygous point mutation in the SASH1 gene (c. 1556G->A) in the affected individual. (b) The regular view (left panels) and melanin pigmentation view of facial images (right panels) from indicated individuals. Images were captured with a VISIA-Complexion Analysis (VISIA-CA) multi-modality facial imaging system. (c) The regular view of hands from an affected individual.