Highly prevalentSERPINB7founder mutation causes pseudodominant inheritance pattern in Nagashima‐type palmoplantar keratosis
Author:
Affiliation:
1. Department of Dermatology Hokkaido University Graduate School of Medicine North 15 West 7, Kita‐ku 060‐8638 Sapporo Japan
2. Department of Dermatology Nagoya University Graduate School of Medicine Nagoya Japan
Funder
Young Scientists B
Scientific Research
Japan Society for the Promotion of Science
Publisher
Wiley
Subject
Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjd.13076
Reference16 articles.
1. “Nagashima-Type” Keratosis as a Novel Entity in the Palmoplantar Keratoderma Category
2. Mutations in SERPINB7, Encoding a Member of the Serine Protease Inhibitor Superfamily, Cause Nagashima-type Palmoplantar Keratosis
3. Atypical nail dystrophy in a possible case of Nagashima-type palmoplantar keratosis
4. Suspected Nagashima‐type palmoplantar keratosis with atypical hyperkeratotic lesions on the ears;Nonomura Y;Eur J Dermatol,2012
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1. A novel SERPINA12 variant and first European patients with diffuse palmoplantar keratoderma;Journal of the European Academy of Dermatology and Venereology;2023-09-22
2. SERPINB7 mutation causes Nagashima‐type palmoplantar keratosis and its spatiotemporal expression in zebrafish;Experimental Dermatology;2023-02-20
3. Nagashima‐type palmoplantar keratoderma: Case series and two novel variants;Pediatric Dermatology;2023-01-31
4. Three new founder mutations in Chinese patients with Nagashima-type palmoplantar keratoderma;British Journal of Dermatology;2022-12-01
5. La génétique des kératodermies palmoplantaires isolées;Annales de Dermatologie et de Vénéréologie - FMC;2022-03
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