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

Y. Kumagai; Noriko Umegaki; T. Sasaki; Y. Nakamura; H. Takahashi; A. Ashida; Y. Tsunemi; M. Kawashima; A. Shimizu; A. Ishiko; K. Nakamura; H. Tsuchihashi; M. Amagai; Akiharu 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, Noriko Umegaki, T. Sasaki, Y. Nakamura, H. Takahashi, A. Ashida, Y. Tsunemi, M. Kawashima, A. Shimizu, A. Ishiko, K. Nakamura, H. Tsuchihashi, M. Amagai, Akiharu Kubo

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

5 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

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1111/jdv.14005

Cite this

Kumagai, Y., Umegaki, 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, Noriko; Sasaki, T. et al.

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, 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

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

author = "Y. Kumagai and Noriko Umegaki and T. Sasaki and Y. Nakamura and H. Takahashi and A. Ashida and Y. Tsunemi and M. Kawashima and A. Shimizu and A. Ishiko and K. Nakamura and H. Tsuchihashi and M. Amagai and Akiharu Kubo",

note = "Funding Information: This work was supported in parts by Practical Research Project for Rare/Intractable Diseases, 16ek0109067h0003, from Japan Agency for Medical Research and Development, AMED.",

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AU - Kumagai, Y.

AU - Umegaki, Noriko

AU - Sasaki, T.

AU - Nakamura, Y.

AU - Takahashi, H.

AU - Ashida, A.

AU - Tsunemi, Y.

AU - Kawashima, M.

AU - Shimizu, A.

AU - Ishiko, A.

AU - Nakamura, K.

AU - Tsuchihashi, H.

AU - Amagai, M.

AU - Kubo, Akiharu

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

ASJC Scopus subject areas

UN SDGs

Access to Document

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