期刊
AMERICAN JOURNAL OF HUMAN GENETICS
卷 73, 期 3, 页码 693-699出版社
UNIV CHICAGO PRESS
DOI: 10.1086/378209
关键词
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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 DSH locus to chromosome 1q21.3. The mutations involved in causing DSH have been identified in the gene that encodes double-stranded RNA-specific adenosine deaminase (DSRAD) as the disease gene.
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