Abstract
New therapeutic hope is emerging for people with the rare inherited blistering skin disease recessive dystrophic epidermolysis bullosa (RDEB). Gurevich et al.1 have reported early-phase clinical trial data evaluating a topical herpes simplex virus 1 vector to restore missing type VII collagen in RDEB skin and heal wounds.
Original language | English |
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Pages (from-to) | 273-275 |
Number of pages | 3 |
Journal | Med |
Volume | 3 |
Issue number | 5 |
DOIs |
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Publication status | Published - 2022 May 13 |
All Science Journal Classification (ASJC) codes
- General Medicine