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John Wiley & Sons Inc

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A recurrent mutation in the KRT17 gene responsible for severe steatocystoma multiplex in a large Chinese family

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John Wiley & Sons Inc

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Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10

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John Wiley & Sons Inc

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Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation location

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Next‐generation sequencing detection and characterization of a heterozygous novel splice junction mutation in the 2B domain of KRT1 in a family with diffuse palmoplantar keratoderma

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