Dyschromatosis symmetrica hereditaria: A case report from Turkey, a new association and a novel gene mutation
Author:
Publisher
Wiley
Subject
Dermatology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1346-8138.2012.01575.x/fullpdf
Reference5 articles.
1. Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis;Suzuki;J Invest Dermatol,2005
2. 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
3. Generalized dyspigmentation on the body;Aliagaoglu;Clin Exp Dermatol,2009
4. Reticulate acropigmentation of Dohi: a report of two new associations;Darouti;Int J Dermatol,2004
5. Achalasia: will genetic studies provide insights?;Gockel;Hum Genet,2010
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1. Dyschromatosis;Harper's Textbook of Pediatric Dermatology;2019-11-20
2. A novel missense mutation in ADAR1 gene causing dyschromatosis symmetrica hereditaria in a Chinese patient;Indian Journal of Dermatology, Venereology, and Leprology;2015
3. A novel nonsense mutation of ADAR1 gene in a Chinese patient with dyschromatosis symmetrica hereditaria;Journal of the European Academy of Dermatology and Venereology;2014-02-14
4. A novel insertion mutation in the ADAR1 gene of a Chinese family with dyschromatosis symmetrica hereditaria;Genetics and Molecular Research;2013
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