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, Shuta Tomida, K. Sakai, S. Fujiwara, Y. Nakamachi, S. Kawano, A. Kawada, K. Nishio, C. Nishigori

Research output: Contribution to journalLetter

9 Citations (Scopus)
Original languageEnglish
Pages (from-to)633-635
Number of pages3
JournalBritish Journal of Dermatology
Volume174
Issue number3
DOIs
Publication statusPublished - Mar 1 2016
Externally publishedYes

ASJC Scopus subject areas

  • Dermatology

Cite this

Epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia : Identification of a recurrent p.P25L mutation in KRT5 in four affected family members. / Nagai, H.; Oiso, N.; Tomida, Shuta; Sakai, K.; Fujiwara, S.; Nakamachi, Y.; Kawano, S.; Kawada, A.; Nishio, K.; Nishigori, C.

In: British Journal of Dermatology, Vol. 174, No. 3, 01.03.2016, p. 633-635.

Research output: Contribution to journalLetter

Nagai, H. ; Oiso, N. ; Tomida, Shuta ; Sakai, K. ; Fujiwara, S. ; Nakamachi, Y. ; Kawano, S. ; Kawada, A. ; Nishio, K. ; Nishigori, C. / Epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia : Identification of a recurrent p.P25L mutation in KRT5 in four affected family members. In: British Journal of Dermatology. 2016 ; Vol. 174, No. 3. pp. 633-635.
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T2 - Identification of a recurrent p.P25L mutation in KRT5 in four affected family members

AU - Nagai, H.

AU - Oiso, N.

AU - Tomida, Shuta

AU - Sakai, K.

AU - Fujiwara, S.

AU - Nakamachi, Y.

AU - Kawano, S.

AU - Kawada, A.

AU - Nishio, K.

AU - Nishigori, C.

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