Loss of the metalloprotease ADAM9 leads to a novel form of cone-rod dystrophy in humans and retinal degeneration in mice

被引：0
|
作者：
Toomes, Carmel [1 ]
Parry, D. A. [1 ]
Bida, L. [2 ]
Towns, K. V. [1 ]
McKibbin, M. [3 ]
Logan, C. V. [1 ]
Ali, M. [1 ]
Bond, J. [1 ]
Saveliev, S. [4 ]
Chance, R. [4 ]
Jacobson, S. G. [4 ]
Springell, K. [1 ]
Adams, M. [1 ]
Banin, E. [2 ]
Johnson, C. A. [1 ]
Sharon, D. [2 ]
Blobel, C. P. [5 ]
Pugh, E. N. [4 ]
Pierce, E. A. [4 ]
Inglehearn, C. F. [1 ]
机构：
[1] Univ Leeds, Leeds Inst Mol Med, Leeds, W Yorkshire, England
[2] Hadassah Hebrew Univ, Med Ctr, Jerusalem, Israel
[3] St James Univ Hosp, Leeds LS9 7TF, W Yorkshire, England
[4] Univ Penn, Sch Med, FM Kirby Ctr Mol Ophthalmol, Philadelphia, PA 19104 USA
[5] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
来源：
JOURNAL OF MEDICAL GENETICS | 2009年 / 46卷
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中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
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页码：S15 / S15
页数：1
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