Novel frameshift mutation of theDSRADgene in a Chinese family with dyschromatosis symmetrica hereditaria
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2008.02632.x/fullpdf
Reference6 articles.
1. 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
2. Refined localization of dyschromatosis symmetrica hereditaria gene to a 9.4-cM region at 1q21-22 and a literature review of 136 cases reported in China;He;Br J Dermatol,2004
3. Reticulate acropigmentation of Dohi: a case report of autosomal recessive inheritance;Alfadley;J Am Acad Dermatol
4. Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21;Zhang;J Invest Dermatol,2003
5. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria;Miyamura;Am J Hum Genet,2003
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1. A Novel P53/POMC/Gas/SASH1 Autoregulatory Feedback Loop and Pathologic Hyperpigmentation;Molecular Medicine;2019-11-06
2. A novel P53/POMC/Gαs/SASH1 autoregulatory feedback loop activates mutated SASH1 to cause pathologic hyperpigmentation;Journal of Cellular and Molecular Medicine;2016-11-25
3. Dyschromatosis symmetrica hereditaria;The Journal of Dermatology;2012-09-14
4. Dyschromatosis symmetrica hereditaria: report of a sporadic case;International Journal of Dermatology;2010-07-19
5. Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria;Archives of Dermatological Research;2010-02-26
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