Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B-Reference-Cited by-同舟云学术

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Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B

Published:2007-02-01 Issue:7 Volume:14 Page:584-594
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Hashimoto T,Gibbs D,Lillo C,Azarian S M,Legacki E,Zhang X-M,Yang X-J,Williams D S

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/3302897.pdf

Reference59 articles.

1. Smith RJ, Berlin CI, Hejtmancik JF, Keats BJ, Kimberling WJ, Lewis RA et al. Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium. Am J Med Genet 1994; 50: 32–38.

2. Keats BJ, Corey DP . The usher syndromes. Am J Med Genet 1999; 89: 158–166.

3. Astuto LM, Weston MD, Carney CA, Hoover DM, Cremers CW, Wagenaar M et al. Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I. Am J Hum Genet 2000; 67: 1569–1574.

4. Bharadwaj AK, Kasztejna JP, Huq S, Berson EL, Dryja TP . Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type I. Exp Eye Res 2000; 71: 173–181.

5. Ouyang XM, Yan D, Du LL, Hejtmancik JF, Jacobson SG, Nance WE et al. Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population. Hum Genet 2005; 116: 292–299.

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