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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