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Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis
2007
200 citations
Journal Article
Field-Weighted Citation Impact:
6.69
Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis | Researchclopedia
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Johannes Gutenberg University Mainz
Monika Beer
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Technical University of Munich
Kerstin Nagel‐Wolfrum
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Johannes Gutenberg University Mainz
Martin McKibbin
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St James's University Hospital
Sharola Dharmaraj
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St Thomas' Hospital
Irma López
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McGill University Health Centre
Lenka Ivings
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St James's University Hospital
G. A. Williams
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St James's University Hospital
Kelly Springell
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St James's University Hospital
C. Geoff Woods
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Addenbrooke's Hospital
Hussain Jafri
Yasmin Abdul Rashid
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King Edward Medical University
Tim M. Strom
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Technical University of Munich
Bert van der Zwaag
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University Medical Center Utrecht
Ilse Gosens
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Radboud University Nijmegen
Ferry F.J. Kersten
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Radboud University Nijmegen
Erwin van Wijk
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Radboud University Medical Center
Joris A. Veltman
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Radboud University Nijmegen
Marijke N. Zonneveld
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Radboud University Nijmegen
Sylvia E. C. van Beersum
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Radboud University Medical Center
Irene H. Maumenee
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Johns Hopkins University
Uwe Wolfrum
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Johannes Gutenberg University Mainz
Michael E. Cheetham
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University College London
Marius Ueffing
Frans P.M. Cremers
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Radboud University Medical Center
Chris F. Inglehearn
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St James's University Hospital
Ronald Roepman
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Radboud University Nijmegen