2024-03-29T01:38:22Z
https://nagoya.repo.nii.ac.jp/oai
oai:nagoya.repo.nii.ac.jp:00030170
2023-01-16T04:23:21Z
499:500:501
A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease
Takeichi, T.
99652
Matsumoto, T.
99653
Nomura, T.
99654
Takeda, M.
99655
Niwa, H.
99656
Kono, M.
99657
Shimizu, H.
99658
Ogi, T.
99659
Akiyama, M.
99660
journal article
Wiley
2020-02
application/pdf
British Journal of Dermatology
2
182
491
493
0007-0963
https://nagoya.repo.nii.ac.jp/record/30170/files/bjd.pdf
eng
https://doi.org/10.1111/bjd.18445
This is the peer reviewed version of the following article: [Takeichi, T., Matsumoto, T., Nomura, T., Takeda, M., Niwa, H., Kono, M., Shimizu, H., Ogi, T. and Akiyama, M. (2020), A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease. Br J Dermatol, 182: 491-493. doi:10.1111/bjd.18445], which has been published in final form at [https://doi.org/10.1111/bjd.18445]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.