作者：
Poulter,J.A. [1]
;
Al-Araimi,M. [2]
;
Conte,I. [3]
;
VanGenderen,M.M. [4]
;
Sheridan,E. [5]
;
Carr,I.M. [6]
;
Parry,D.A. [7]
;
Shires,M. [8]
;
Carrella,S. [9]
;
Bradbury,J. [10]
;
Khan,K. [11]
;
Lakeman,P. [12]
;
Sergouniotis,P.I. ;
Webster,A.R. ;
Moore,A.T. ;
Pal,B. ;
Mohamed,M.D. ;
Venkataramana,A. ;
Ramprasad,V. ;
Shetty,R. ;
Saktivel,M. ;
Kumaramanickavel,G. ;
Tan,A. ;
Mackey,D.A. ;
Hewitt,A.W. ;
Banfi,S. ;
Ali,M. ;
Inglehearn,C.F. ;
Toomes,C.
作者单位：
Bartiméus, Institute for the Visually Impaired, Zeist 3700 BA, Netherlands
[1]
Division of Inherited Eye Disease, Institute of Ophthalmology, University College London, London
[2]
Department of Ophthalmology, Bradford Royal Infirmary, Bradford, West Yorkshire BD9 6RJ, United
[3]
Department of Ophthalmology, St. Thomas' Hospital, London SE1 9RT, United Kingdom
[4]
SciGenom Labs, Cochin, Kerala 682037, India
[5]
Leeds Institute of Molecular Medicine, University of Leeds, Leeds, West Yorkshire LS9 7TF, United
[6]
Telethon Institute of Genetics and Medicine, Naples 80131, Italy, Medical Genetics, Department of
[7]
Department of Clinical Genetics, VU University Medical Center, Amsterdam NL-1081 HV, Netherlands
[8]
Centre for Ophthalmology and Visual Science, University of Western Australia, Crawley, Perth WA
[9]
Department of Ocular Genetics, Narayana Nethralaya, Bangalore, Karnataka 560099, India
[10]
Telethon Institute of Genetics and Medicine, Naples 80131, Italy
[11]
Moorfields Eye Hospital, London EC1V 2PD, United Kingdom
[12]
发布时间
2014-03-14
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