Abstract
We report a case of epidermolysis bullosa simplex (EBS) associated with a family cluster of EBS and a novel KRT5 mutation. The case is presented in the context of recent advances in the study of the disease.
Original language | English (US) |
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Pages (from-to) | 1 |
Number of pages | 1 |
Journal | Dermatology Online Journal |
Volume | 18 |
Issue number | 6 |
State | Published - 2012 |
ASJC Scopus subject areas
- Dermatology