Novel corneodesmosin null mutation and entire gene deletion in two families with inflammatory peeling skin syndrome

被引：0
|
作者：
Furio, L. [1 ,2 ]
Honma, H. [8 ]
Deraison, C. [3 ]
Robin, A. [3 ]
Tron, E. [4 ]
Sans, B. [5 ]
Gardini-Fournie, E. [6 ]
Igawa, S. [8 ]
Murakami, M. [8 ]
Prost, C. [7 ]
Ishida-Yamamoto, A. [8 ]
Hovnanian, A. [1 ,2 ,5 ]
机构：
[1] INSERM, U781, Paris, France
[2] Univ Paris 05, Paris, France
[3] Fac Med Toulouse, INSERM, U563, F-31073 Toulouse, France
[4] Hop Necker Enfants Malad, Dept Genet, Paris, France
[5] Castres Hosp, Dept Dermatol, Castres, France
[6] Purpan Hosp, Dept Gastroenterol, Toulouse, France
[7] Univ Paris 13, Histol Lab, Paris, France
[8] Asahikawa Med Univ, Dept Dermatol, Asahikawa, Hokkaido, Japan
来源：
JOURNAL OF INVESTIGATIVE DERMATOLOGY | 2011年 / 131卷
关键词：
D O I：
暂无
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
410
引用
收藏
页码：S69 / S69
页数：1
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