The clinical spectrum of epidermolysis bullosa simplex
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2133.2000.03358.x/fullpdf
Reference32 articles.
1. The prevalence of epidermolysis bullosa in Scotland.;Horn;Br J Dermatol,1997
2. Partial dominance of a keratin 14 mutation in epidermolysis bullosa simplex-increased severity of disease in a homozygote.;Hu;J Invest Dermatol,1997
3. Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex.;Corden;Hum Mutat,1998
4. Human keratin diseases: hereditary fragility of specific epithelial tissues.;Corden;Exp Dermatol,1996
5. Plectin abnormality in epidermolysis bullosa simplex Ogna: non-responsiveness of basal keratinocytes to some anti-rat plectin antibodies.;Koss-Harnes;Exp Dermatol,1997
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