Loss-of-function variants in KLF4 underlie autosomal dominant palmoplantar keratoderma
Author:
Funder
Israel Science Foundation
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference40 articles.
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2. Hereditary palmoplantar keratodermas. Part II: syndromic palmoplantar keratodermas - diagnostic algorithm and principles of therapy;Guerra;J Eur Acad Dermatol Venereol,2018
3. Diffuse nonepidermolytic palmoplantar keratoderma caused by a recurrent nonsense mutation in DSG1;Keren;Arch Dermatol,2005
4. Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening;Lovgren;Br J Dermatol,2017
5. Focal palmoplantar keratoderma caused by an autosomal dominant inherited mutation in the desmoglein 1 gene;Milingou;Dermatology,2006
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