Mosaic expression of uncein and 180-kDa bullous pemphigoid antigen in generalized atrophic benign epidermolysis bullosa
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.1997.tb03666.x/fullpdf
Reference33 articles.
1. A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering
2. A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex
3. Molecular basis for the dystrophic forms of epidermolysis bullosa: mutations in the type VII collagen gene
4. Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ–5)
5. Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia
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1. 6 The vesiculobullous reaction pattern;Weedon's Skin Pathology;2010
2. The vesiculobullous reaction pattern;Weedon's Skin Pathology;2010
3. Revertant mosaicism: partial correction of a germ-line mutation in COL17A1 by a frame-restoring mutation;Journal of Clinical Investigation;1999-05-15
4. Mosaic expression of uncein, linear IgA bullous dermatosis antigen and 180‐kDa bullous pemphigoid antigen in generalized atrophic benign epidermolysis bullosa;British Journal of Dermatology;1998-05
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