Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5

Y. Kumagai; N. Umegaki-Arao; T. Sasaki; Y. Nakamura; H. Takahashi; A. Ashida; Y. Tsunemi; M. Kawashima; A. Shimizu; A. Ishiko; K. Nakamura; H. Tsuchihashi; M. Amagai; A. Kubo

doi:10.1111/jdv.14005

Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5

Y. Kumagai, N. Umegaki-Arao, T. Sasaki, Y. Nakamura, H. Takahashi, A. Ashida, Y. Tsunemi, M. Kawashima, A. Shimizu, A. Ishiko, K. Nakamura, H. Tsuchihashi, M. Amagai, A. Kubo

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

2 Citations (Scopus)

Original language	English
Pages (from-to)	e241-e243
Journal	Journal of the European Academy of Dermatology and Venereology
Volume	31
Issue number	5
DOIs	https://doi.org/10.1111/jdv.14005
Publication status	Published - 2017 May

ASJC Scopus subject areas

Dermatology
Infectious Diseases

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10.1111/jdv.14005

Cite this

Kumagai, Y., Umegaki-Arao, N., Sasaki, T., Nakamura, Y., Takahashi, H., Ashida, A., Tsunemi, Y., Kawashima, M., Shimizu, A., Ishiko, A., Nakamura, K., Tsuchihashi, H., Amagai, M., & Kubo, A. (2017). Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5. Journal of the European Academy of Dermatology and Venereology, 31(5), e241-e243. https://doi.org/10.1111/jdv.14005

Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5. / Kumagai, Y.; Umegaki-Arao, N.; Sasaki, T.; Nakamura, Y.; Takahashi, H.; Ashida, A.; Tsunemi, Y.; Kawashima, M.; Shimizu, A.; Ishiko, A.; Nakamura, K.; Tsuchihashi, H.; Amagai, M.; Kubo, A.

In: Journal of the European Academy of Dermatology and Venereology, Vol. 31, No. 5, 05.2017, p. e241-e243.

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

Kumagai, Y, Umegaki-Arao, N, Sasaki, T , Nakamura, Y , Takahashi, H, Ashida, A, Tsunemi, Y, Kawashima, M, Shimizu, A, Ishiko, A, Nakamura, K, Tsuchihashi, H, Amagai, M & Kubo, A 2017, 'Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5', Journal of the European Academy of Dermatology and Venereology, vol. 31, no. 5, pp. e241-e243. https://doi.org/10.1111/jdv.14005

Kumagai, Y. ; Umegaki-Arao, N. ; Sasaki, T. ; Nakamura, Y. ; Takahashi, H. ; Ashida, A. ; Tsunemi, Y. ; Kawashima, M. ; Shimizu, A. ; Ishiko, A. ; Nakamura, K. ; Tsuchihashi, H. ; Amagai, M. ; Kubo, A. / Distinct phenotype of epidermolysis bullosa simplex with infantile migratory circinate erythema due to frameshift mutations in the V2 domain of KRT5. In: Journal of the European Academy of Dermatology and Venereology. 2017 ; Vol. 31, No. 5. pp. e241-e243.

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