First report of the coexistence of dyschromatosis symmetrica hereditaria and psoriasis: one novel TCT to A mutation in the double-RNA-specific adenosine deaminase gene
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2011.04096.x/fullpdf
Reference9 articles.
1. Genetics of pigmentary disorders;Tomita;Am J Med Genet C Semin Med Genet,2004
2. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria;Miyamura;Am J Hum Genet,2003
3. An association study of 22 candidate genes in psoriasis families reveals shared genetic factors with other autoimmune and skin disorders;Oudot;J Invest Dermatol,2009
4. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases;Oyama;Br J Dermatol,1999
5. Complexity of the association between psoriasis and comorbidities;Nijsten;J Invest Dermatol,2009
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1. Novel ADAR1 mutations in three cases of psoriasis coexisting with dyschromatosis symmetrica hereditaria;Journal of the European Academy of Dermatology and Venereology;2021-09
2. Dyschromatosis symmetrica hereditaria with cutaneous lupus erythematosus and hyperthyroidism;International Medical Case Reports Journal;2017-05
3. Two novel ADAR1 gene mutations in two patients with dyschromatosis symmetrical hereditaria from birth;Molecular Medicine Reports;2017-04-03
4. Two novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria successfully treated with fractional CO2 laser;Journal of the European Academy of Dermatology and Venereology;2015-03-12
5. Two novel mutations in the DSRAD gene in two Chinese pedigrees with dyschromatosis symmetrica hereditaria;European Journal of Dermatology;2013-11
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