Ichthyosis, Follicular Atrophoderma, And Hypotrichosis Caused By Mutations In ST14 Is Associated With Impaired Profilaggrin Processing

    Thomas Alef, Serena Torres, Ingrid Haußer, Dieter Metze, Ümit Türsen, Gilles G. Lestringant, Hans Christian Hennies
    Studysummary This study identified genetic mutations linked to congenital ichthyosis in families from the UAE and Turkey, revealing a connection between keratinization disorders and impaired filaggrin processing.
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