Author:
Kono Michihiro,Okamoto Takashi,Takeichi Takuya,Muro Yoshinao,Akiyama Masashi
Reference10 articles.
1. Miyamura Y, Suzuki T, Kono M, et al. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria. Am J Hum Genet 2003; 73: 693–9.
2. Kobayashi T, Kono M, Suganuma M, et al. Analysis of genotype/phenotype correlations in Japanese patients with dyschromatosis symmetrica hereditaria. Nagoya J Med Sci 2018; 80: 267–77.
3. Kono M, Matsumoto F, Suzuki Y, et al. Dyschromatosis symmetrica hereditaria and Aicardi-Goutieres syndrome 6 are phenotypic variants caused by ADAR1 mutations. J Invest Dermatol 2016; 136: 875–8.
4. Kawakami T, Otaguchi R, Kyoya M, Soma Y, Suzuki T. Patient with dyschromatosis symmetrica hereditaria treated with miniature punch grafting, followed by excimer light therapy. J Dermatol 2013; 40: 771–2.
5. Xu XG, Lv Y, Zhai JL, Li YH, Gao XH, Chen HD. Two novel mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria successfully treated with fractional CO2 laser. J Eur Acad Dermatol Venereol 2016; 30: 1035–8.
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献