Intracerebroventricular gene therapy that delays neurological disease progression is associated with selective preservation of retinal ganglion cells in a canine model of CLN2 disease
| Autor: | Whiting, Rebecca E.H. a, Jensen, Cheryl A. a, Pearce, Jacqueline W. b, Gillespie, Lauren E. a, Bristow, Daniel E. c, Katz, Martin L. a, ∗ |
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| Zdroj: | In Experimental Eye Research May 2016 146:276-282 |
| Databáze: | ScienceDirect |
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