A novel deletion mutation of the DSRAD gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria

Volume: 153, Issue: 5, Pages: 1064 - 1066
Published: Nov 1, 2005
Abstract
Conflicts of interest: None declared. Dyschromatosis symmetrica hereditaria (DSH; reticulate acropigmentation of Dohi,1 symmetric dyschromatosis of the extremities, leucopathia punctata et reticularis symmetrica,2 acropigmentatio symmetrica Dohi–Komaya;3 OMIM 127400) is a pigmentary genodermatosis characterized by onset in infancy or early childhood of a mixture of hyperpigmented and hypopigmented macules of various sizes on the dorsal aspects...
Paper Details
Title
A novel deletion mutation of the DSRAD gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria
Published Date
Nov 1, 2005
Volume
153
Issue
5
Pages
1064 - 1066
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