Additional causal SNRPE mutations in hereditary hypotrichosis simplex

被引：5
|
作者：
Pan, C. [1 ,2 ]
Humbatova, A. [3 ,4 ]
Zheng, L. [1 ,2 ]
Cesarato, N. [3 ,4 ]
Grimm, C. [5 ]
Chen, F. [1 ,2 ]
Blaumeiser, B. [6 ]
Catalan-Lamban, A. [7 ]
Patino-Garcia, A. [7 ]
Fischer, U. [5 ]
Cheng, R. [1 ]
Li, Y. [1 ,2 ]
Yu, X. [1 ]
Yao, Z. [1 ,2 ]
Li, M. [1 ,2 ,8 ]
Betz, R. C. [3 ,4 ]
机构：
[1] Xinhua Hosp, Dept Dermatol, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Inst Dermatol, Shanghai, Peoples R China
[3] Univ Bonn, Sch Med, Inst Human Genet, Bonn, Germany
[4] Univ Hosp Bonn, Bonn, Germany
[5] Univ Wurzburg, Dept Biochem, Wurzburg, Germany
[6] Univ Antwerp, Dept Med Genet, Antwerp, Belgium
[7] Clin Univ Navarra, Dept Pediat, Pamplona, Spain
[8] Ctr Rare Dis Diag, Shanghai, Peoples R China
来源：
BRITISH JOURNAL OF DERMATOLOGY | 2021年 / 185卷 / 02期
关键词：
D O I：
10.1111/bjd.20089
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
引用
收藏
页码：439 / 441
页数：4
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