A Case of Hailey-Hailey Disease in an Infant with a New ATP2C1 Gene Mutation
Author:
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1525-1470.2010.01088.x/fullpdf
Reference11 articles.
1. Familial benign chronic pemphigus. Report of 13 cases in 4 generations of a family and report of 9 additional cases in 4 generations of a family;Hailey;Arch Dermatol Syphilol,1939
2. Generalized Hailey-Hailey disease;Marsch;Br J Dermatol,1978
3. Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease;Hu;Nat Genet,2000
4. Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump;Sudbrak;Hum Mol Genet,2000
5. Localization of the gene whose mutations underlie Hailey-Hailey disease to chromosome 3q;Ikeda;Hum Mol Genet,1994
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3. Familial “benign” pemphigus? Erythroderma and fatal outcome;Anais Brasileiros de Dermatologia;2020-01
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