Mutations in AAGAB underlie autosomal dominant punctate palmoplantar keratoderma
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Detection of Nuclear Blebbing and DNA Leakage in Mammalian Cells by Immunofluorescence
Published on: January 17, 2025
1Department of Dermatology, Worthing Hospital, Western Hospitals NHS Trust, Worthing, West Sussex, UK.
Abstract:
Punctate palmoplantar keratoderma type 1 (PPPK1) is a rare autosomal dominant inherited skin disease, characterized by multiple hyperkeratotic lesions on the palms and soles. The causative gene for PPPK1 has been identified as AAGAB, which encodes α- and γ-adaptin-binding protein p34. We describe the clinical features in three unrelated families with PPPK1, and report three recurrent causative mutations in AAGAB.
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