SERPINB7 novel mutation in Chinese patients with Nagashima‐type palmoplantar keratosis and cases associated with atopic dermatitis
Author:
Affiliation:
1. Beijing Children’s Hospital Capital Medical University Beijing China
2. Department of Dermatology Inner Mongolia People’s Hospital Huhhot China
Funder
The Special Fund of the Pediatric Medical Coordinated Development Center of Beijing Hospital Authority
Publisher
Wiley
Subject
Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijd.14901
Reference5 articles.
1. Mutations in SERPINB7, Encoding a Member of the Serine Protease Inhibitor Superfamily, Cause Nagashima-type Palmoplantar Keratosis
2. Highly prevalentSERPINB7founder mutation causes pseudodominant inheritance pattern in Nagashima‐type palmoplantar keratosis
3. Three cases of Nagashima-type palmoplantar keratosis associated with atopic dermatitis: A diagnostic pitfall
4. ‘Nagashima-type’ keratosis palmoplantaris in two siblings
5. Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy
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1. Genetic analysis of seven patients with inherited ichthyosis and Nagashima‑type palmoplantar keratoderma;Molecular Medicine Reports;2024-05-01
2. Application of topical gentamicin ointment in the treatment of Nagashima‐type palmoplantar keratosis in children with a nonsense mutation;Pediatric Investigation;2023-06-28
3. SERPINB7 mutation causes Nagashima‐type palmoplantar keratosis and its spatiotemporal expression in zebrafish;Experimental Dermatology;2023-02-20
4. La génétique des kératodermies palmoplantaires isolées;Annales de Dermatologie et de Vénéréologie - FMC;2022-03
5. Nagashima-Type Palmoplantar Keratosis: Clinical Characteristics, Genetic Characterization, and Clinical Management;BioMed Research International;2021-01-27
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