Associated Papers
Seven novel mutations of ADAR in multi-ethnic pedigrees with dyschromatosis symmetrica hereditaria in China.
Wang P et al.
Molecular Genetics & Genomic Medicine, 2019
Double-stranded RNA-specific adenosine deaminase (DSRAD) gene mutation in a Chinese family with dyschromatosis symmetrica hereditaria (DSH).
Dong Y et al.
International Journal of Dermatology, 2011
A missense mutation c.G2747A (p.R916Q) of ADAR1 gene in dyschromatosis symmetrica hereditaria is not a novel mutation.
Hayashi M et al.
Archives of Dermatological Research, 2010
Mutational spectrum of the ADAR1 gene in dyschromatosis symmetrica hereditaria.
Li M et al.
Archives of Dermatological Research, 2010
Ten novel mutations of the ADAR1 gene in Japanese patients with dyschromatosis symmetrica hereditaria.
Suzuki N et al.
The Journal of Investigative Dermatology, 2007
Five novel mutations of RNA-specific adenosine deaminase gene with dyschromatosis symmetrica hereditaria.
Hou Y et al.
Acta Dermato-venereologica, 2007
Two novel mutations and evidence for haploinsufficiency of the ADAR gene in dyschromatosis symmetrica hereditaria.
Liu Q et al.
The British Journal of Dermatology, 2006
Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis.
Suzuki N et al.
The Journal of Investigative Dermatology, 2005
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