Keratin 9 mutations in the coil 1A region in epidermolytic palmoplantar keratoderma.

Abstract excerpt

The palmoplantar keratodermas (PPK) are a heterogeneous group of conditions, most frequently inherited in autosomal dominant fashion. A few are well-documented autosomal recessive disorders; other are acquired in association with certain metabolic disorders and malignancies. Recently different point mutations of the keratin 9 (K9) gene have been identified in unrelated families with epidermolytic palmoplantar...

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Child
• Share to DNA Primers
• Share to Epidermis