Article
Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria.
American journal of human genetics - 1 Sept 2003
Miyamura Yoshinori, Suzuki Tamio, Kono Michihiro, Inagaki Katsuhiko, Ito Shiro, Suzuki Noriyuki, Tomita Yasushi
Abstract excerpt
Dyschromatosis symmetrica hereditaria (DSH) (also called "reticulate acropigmentation of Dohi") is a pigmentary genodermatosis of autosomal dominant inheritance characterized by a mixture of hyperpigmented and hypopigmented macules distributed on the dorsal aspects of the hands and feet. To determine the gene responsible for this disease, we performed a genomewide search in three families with DSH and mapped the...
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