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/10.1046/j.1365-2133.1997.6701619.x/fullpdf
Reference33 articles.
1. A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering;Lane;Nature,1992
2. A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex;Hovnanian;Nature Genet,1993
3. Molecular basis for the dystrophic forms of epidermolysis bullosa: mutations in the type VII collagen gene;Uitto;Arch Dermatol Res,1994
4. Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ-5);Aberdam;Nature Genet,1994
5. Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia;Vidal;Nature Genet,1995
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