A novel keratin 5 mutation in a familial cluster

Hadar Lev-Tov1, Raja K Sivamani, Barbara Burrall

  • 1Department of Dermatology, University of California at Davis, CA, USA.

Summary

We identified a new KRT5 gene mutation causing epidermolysis bullosa simplex (EBS), a rare skin disorder. This finding is significant for understanding familial EBS cases and advancing disease research.

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