Epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia: Identification of a recurrent p.P25L mutation in KRT5 in four affected family members

H. Nagai, N. Oiso, S. Tomida, K. Sakai, S. Fujiwara, Y. Nakamachi, S. Kawano, A. Kawada, K. Nishio, C. Nishigori

Research output: Contribution to journal › Letter › peer-review

13 Citations (Scopus)

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