Mutations of ATP2C1 in Japanese Patients with Hailey–Hailey Disease: Intrafamilial and Interfamilial Phenotype Variations and Lack of Correlation with Mutation Patterns
- 1 December 2001
- journal article
- research article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 117 (6) , 1654-1656
- https://doi.org/10.1046/j.0022-202x.2001.01596.x
Abstract
No abstract availableKeywords
Funding Information
- Japanese Dermatological Association
- Smithsonian Institution
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 8 references indexed in Scilit:
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- Hailey-Hailey Disease Maps to a 5 cM Interval on Chromosome 3q21-q24Journal of Investigative Dermatology, 1995
- Localization of the gene whose mutations underlie Hailey—Hailey disease to chromosome 3qHuman Molecular Genetics, 1994
- Linkage of the Epidermolytic Hyperkeratosis Phenotype and the Region of the Type II Keratin Gene Cluster on Chromosome 12Journal of Investigative Dermatology, 1992
- Hailey–Hailey disease: the clinical features, response to treatment and prognosisBritish Journal of Dermatology, 1992