Inherited palmoplantar keratoderma and sensorineural deafness associated with A7445G point mutation in the mitochondrial genome
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2133.2000.03797.x/fullpdf
Reference42 articles.
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2. Palmoplantar keratoderma and associated syndromes;Itin;Semin Dermatol,1995
3. Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24;Stevens;Arch Dermatol,1996
4. Genes encoding structural proteins of epidermal cornification and S100 calcium-binding proteins form a gene complex (‘epidermal differentiation complex’) on human chromosome 1q21;Mischke;J Invest Dermatol,1996
5. A mutation in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratoderma;Kimonis;J Invest Dermatol,1994
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