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

doi:10.1111/bjd.14083

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

Original language	English
Pages (from-to)	633-635
Number of pages	3
Journal	British Journal of Dermatology
Volume	174
Issue number	3
DOIs	https://doi.org/10.1111/bjd.14083
Publication status	Published - Mar 1 2016
Externally published	Yes

ASJC Scopus subject areas

Dermatology

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Nagai, H., Oiso, N., Tomida, S., Sakai, K., Fujiwara, S., Nakamachi, Y., Kawano, S., Kawada, A., Nishio, K., & Nishigori, C. (2016). Epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia: Identification of a recurrent p.P25L mutation in KRT5 in four affected family members. British Journal of Dermatology, 174(3), 633-635. https://doi.org/10.1111/bjd.14083

Nagai, H, Oiso, N, Tomida, S, Sakai, K, Fujiwara, S, Nakamachi, Y, Kawano, S, Kawada, A, Nishio, K & Nishigori, C 2016, 'Epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia: Identification of a recurrent p.P25L mutation in KRT5 in four affected family members', British Journal of Dermatology, vol. 174, no. 3, pp. 633-635. https://doi.org/10.1111/bjd.14083

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

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

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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, S.

AU - Sakai, K.

AU - Fujiwara, S.

AU - Nakamachi, Y.

AU - Kawano, S.

AU - Kawada, A.

AU - Nishio, K.

AU - Nishigori, C.

PY - 2016/3/1

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

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