Mental Retardation Associated With Retinitis Pigmentosa in the Xp11.3 Deletion Syndrome: ZNF674 in the Dock. Guilty or Innocent?

被引：0
|
作者：
Kaplan, J. [1 ]
Delphin, N. [1 ]
Bonneau, D. [2 ]
Zanloghi, X. [3 ]
Gerber, S. [1 ]
Bonnefont, J-P. [1 ]
Dufier, J-L. [4 ]
Roche, O. [4 ]
Rozet, J-M. [1 ]
机构：
[1] Paris Descartes Univ, CHU Necker, INSERM, Genet,U781, Paris, France
[2] Univ Angers, INSERM, U694, Biochem Genet, Angers, France
[3] Clin Sourdille, Ophthol, Nantes, France
[4] Paris Descartes Univ, CHU Necker, Ophthalmol, Paris, France
来源：
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2010年 / 51卷 / 13期
关键词：
retina; retinal degenerations: hereditary; positional cloning;
D O I：
暂无
中图分类号：
R77 [眼科学];
学科分类号：
100212 ;
摘要：
4082
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页数：4
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