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Fig. 3 | Orphanet Journal of Rare Diseases

Fig. 3

From: Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients

Fig. 3

Distribution of the mutations in our patient series, along the gDNA of FERMT1. In the X axis, it is represented by the length of the FERMT1 gene, considering the + 1 position as the ATG. For that reason, the gene is from − 3990 to + 44709 positions. The Y-axis, shows the number of patients presenting with each mutation, in orange (free of SCC) and in blue (developed SCC). Four patients with no mutational information available were excluded from this figure

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172