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FGFR3 and PIK3CA mutations in stucco keratosis and dermatosis papulosa nigra
British Journal of Dermatology, 10/26/09

Hafner C et al. – The results indicate that FGFR3 and PIK3CA mutations are involved in the pathogenesis of STK and DPN. The molecular genetic findings furthermore support the concept that both skin lesions are specific variants of seborrhoeic keratosis, sharing a common genetic background.

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