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Updated: Sep 25, 2026

Isolation and Culture of Adult Epithelial Stem Cells from Human Skin
Published on: March 31, 2011
A Japanese case of de novo dominant dystrophic epidermolysis bullosa
S Matsuba1, Y Suga, N Mayuzumi
1Department of Dermatology, Juntendo University School of Medicine, Tokyo Japan. matsuba@med.juntendo.ac.jp
Abstract:
We report a Japanese case of dominant dystrophic epidermolysis bullosa with a de novo mutation in the triple-helical domain of the type VII collagen. Mutation detection revealed a glycine --> aspartic acid substitution at amino acid position 2012 in exon 73 (G2012D). This previously unreported mutation underlies a clinical phenotype of moderately severe, localized skin blistering.
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