Mutations in the ATP2C1 gene in Chinese patients with Hailey–Hailey disease
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2230.2006.02204.x/fullpdf
Reference12 articles.
1. FAMILIAL BENIGN CHRONIC PEMPHIGUS
2. Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
3. Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump
4. Immunohistochemical Distribution of CD44 and Desmoplakin I & II in Hailey-Hailey's Disease and Darier's Disease
5. Involvement of the adherens junction - actin filament system in acantholytic dyskeratosis of Hailey-Hailey disease. A histological, ultrastructural, and histochemical study of lesional and non-lesional skin
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1. Hailey-Hailey Disease (Familial Benign Chronic Pemphigus);Atlas of Male Genital Dermatology;2018-11-13
2. Identification of 2 Novel Mutations in ATP2C1 Gene in Hailey-Hailey Disease and a Literature Review of Variations in a Chinese Han Population;Medical Science Monitor Basic Research;2017-11-06
3. ATP2C1 gene mutations in Hailey–Hailey disease and possible roles of SPCA1 isoforms in membrane trafficking;Cell Death & Disease;2016-06
4. Mutations of transglutaminase-1 in Chinese patients with autosomal recessive congenital ichthyosis: a case report with clinical and genetic analysis of Chinese cases reported in literature;Clinical and Experimental Dermatology;2014-08-22
5. 9 Disorders of epidermal maturation and keratinization;Weedon's Skin Pathology;2010
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