A novel mouse model for complete Congenital Stationary Night Blindness (cCSNB)

被引：0
|
作者：
Neuille, Marion [1 ,2 ,3 ]
El Shamieh, Said [1 ,2 ,3 ]
Orhan, Elise [1 ,2 ,3 ]
Michiels, Christelle [1 ,2 ,3 ]
Bujakowska, Kinga Maria [1 ,2 ,3 ,4 ]
Poch, Olivier [5 ,6 ]
Sahel, Jose Alain [2 ,3 ,7 ,8 ,9 ,10 ,11 ]
Audo, Isabelle [2 ,3 ,7 ,8 ,11 ]
Zeitz, Christina [1 ,2 ,3 ]
机构：
[1] Univ Pierre & Marie Curie Paris 6, Inst Vis, Paris, France
[2] INSERM, UMR S968, Paris, France
[3] CNRS, UMR 7210, Paris, France
[4] Massachusetts Eye & Ear Infirm, Ocular Genom Inst, Boston, MA 02114 USA
[5] Integrat Bioinformat & Genom Lab ICube, Strasbourg, France
[6] CNRS, UMR 7357, Strasbourg, France
[7] Univ Pierre & Marie Curie Paris 6, Paris, France
[8] INSERM, CHNO, DHOS, CIC 503, Paris, France
[9] Fdn Ophtalmol Adolphe de Rothschild, Paris, France
[10] Acad Sci Inst France, Paris, France
[11] UCL Inst Ophthalmol, London, England
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2014年 / 55卷 / 13期
关键词：
563 inner retina dysfunction: hereditary; 435 bipolar cells; 510 electroretinography: non-clinical;
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
1642
引用
收藏
页数：4
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