Identification of a novel mutation in the DSRAD gene in a Chinese family with dyschromatosis symmetrica hereditaria

被引：5

作者：

Pan, Huaining ^{[1
]}

Wang, Zizheng ^{[1
]}

He, Bangshun ^{[1
]}

Chen, Chen ^{[1
]}

Hong, Bing ^{[1
]}

Chen, Wenqi ^{[1
]}

Ji, Chao ^{[1
]}

He, Shaoheng ^{[1
]}

Wang, Shukui ^{[1
]}

Chen, Xingguo ^{[1
]}

机构：

[1] Nanjing Med Univ, Dept Dermatol, Nanjing Hosp 1, Nanjing 210006, Peoples R China

来源：

JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY | 2010年 / 63卷 / 03期

关键词：

D O I：

10.1016/j.jaad.2009.08.065

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

[No abstract available]

引用

收藏

页码：529 / 530

页数：2

相关论文

共 3 条

[1] Identification of two novel mutations in Chinese patients with Dyschromatosis symmetrica hereditaria
Li, M
Li, CR
Hua, HK
Zhu, WY
Lu, Y
Yang, LJ
[J]. ARCHIVES OF DERMATOLOGICAL RESEARCH, 2005, 297 (05) : 196 - 200
[2] Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria
Miyamura, Y
Suzuki, T
Kono, M
Inagaki, K
Ito, S
Suzuki, N
Tomita, Y
[J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (03) : 693 - 699
[3] Acquired brachial cutaneous dyschromatosis: A common pigmentary disorder of the arm in middle-aged women
Rongioletti, F
Rebora, A
[J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2000, 42 (04) : 680 - 684