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

研究成果 › 査読

本文言語	English
ページ（範囲）	633-635
ページ数	3
ジャーナル	British Journal of Dermatology
巻	174
号	3
DOI	https://doi.org/10.1111/bjd.14083
出版ステータス	Published - 3月 1 2016
外部発表	はい

ASJC Scopus subject areas

皮膚病学

文献へのアクセス

10.1111/bjd.14083

他のファイルとリンク

引用スタイル

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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