A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease

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Bibliographic Details
Published in:	British journal of dermatology (1951) Vol. 182; no. 2; pp. 491 - 493
Main Authors:	Takeichi, T., Matsumoto, T., Nomura, T., Takeda, M., Niwa, H., Kono, M., Shimizu, H., Ogi, T., Akiyama, M.
Format:	Journal Article
Language:	English
Published:	England Oxford University Press 01-02-2020
Subjects:	Adult Amyloid Precursor Protein Secretases - genetics Hidradenitis Suppurativa - genetics Humans Keratinization Male Membrane Glycoproteins - genetics Missense mutation Mutation, Missense Protein Domains Protein Sorting Signals
Online Access:	Get full text
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ISSN:	0007-0963 1365-2133
DOI:	10.1111/bjd.18445