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Gene therapy for Leber congenital amaurosis: advances and future directions

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Year: 2012
Type: article
Source: Graefe s Archive for Clinical and Experimental Ophthalmology
DOI: 10.1007/s00417-012-2028-2
Authors: Robert B. Hufnagel, Zubair M. Ahmed, Zélia M. Corrêa, Robert A. Sisk
Institutions: Cincinnati Children's Hospital Medical Center, University of Cincinnati, University of Cincinnati Medical Center, Cincinnati Eye Institute
Language: English

Topic: Retinal Development and Disorders
Subfield: Molecular Biology
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: green

Funders: Research to Prevent Blindness, National Institutes of Health, National Institute on Deafness and Other Communication Disorders
Awards: MOLECULAR GENETICS OF USHER SYNDROME TYPE I, G7358535774
OpenAlex ID: W1995649219
FWCI: 3.207
Cites: 77
Cited by: 44
Related to: 10
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