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. Author manuscript; available in PMC: 2014 Dec 1.
Published in final edited form as: Int J Dermatol. 2013 May 15;53(6):692–698. doi: 10.1111/ijd.12008

Figure 3.

Figure 3

Family pedigree (a), and mutation analysis demonstrating the presence of R1141X mutation (b). The proband (I-2; arrow) is homozygous for the mutation, while the husband of the proband (I-1) shows wild type sequence, R1141. The three children (II-1,2,3) are heterozygous carriers of the mutation.