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Epidermolysis bullosa nevus arising in a patient with Dowling–Meara type epidermolysis bullosa simplex with a novel K5 mutation
Journal of Dermatology, 08/07/09
Sugiyama–Fukamatsu H et al. – The pigmented lesions revealed histopathological features of compound nevus without malignant changes. Gene analysis revealed an E478K (Glu to Lys) mutation in exon 5 of the keratin 5 (K5) gene. These findings, together with clinical features, were consistent with those of Dowling–Meara type EB associated with so–called EB nevus.
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