Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2133.2001.03950.x/fullpdf
Reference20 articles.
1. Epidermolysis bullosa simplex and mottled pigmentation: a new dominant syndrome. I. Clinical and histological features;Fischer;Clin Genet,1979
2. Speckled hyperpigmentation, palmoplantar punctate keratoses and childhood blistering: a clinical triad, with variable associations. A report of two families;Boss;Br J Dermatol,1981
3. Epidermolysis bullosa simplex with mottled pigmentation;Coleman;Br J Dermatol,1993
4. Epidermolysis bullosa simplex with mottled pigmentation. Case report and review of the literature;Combemale;Dermatol,1994
5. A mutation in the V1 domain of keratin 5 causes epidermolysis bullosa simplex with mottled pigmentation;Irvine;J Invest Dermatol,1997
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