Barbora Jerábková

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BACKGROUND Epidermolysis bullosa simplex (EBS) is an inherited skin disorder caused by mutations in the keratin 5 (KRT5) and keratin 14 (KRT14) genes, with fragility of basal keratinocytes leading to epidermal cytolysis and blistering. OBJECTIVES In this study, we characterized mutations in KRT5 and KRT14 genes in patients with EBS and investigated their(More)
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