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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