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

页数：4

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