Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness

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作者： Scalabrino, Miranda L. ^[1] ; Boye, Sanford L. ^[2] ; Fransen, Kathryn M. H. ^[3] ; Noel, Jennifer M. ^[4] ; Dyka, Frank M. ^[5] ; Min, Seok Hong ; Ruan, Qing ; De Leeuw, Charles N. ; Simpson, Elizabeth M. ; Gregg, Ronald G. ; McCall, Maureen A. ; Peachey, Neal S. ; Boye, Shannon E.

作者单位： Univ Florida, Coll Med, Dept Ophthalmol, Gainesville, FL 32610 USA ^[1] Univ British Columbia, Ctr Mol Med & Therapeut, Child & Family Res Inst, Vancouver, BC V5Z 4H4 ^[2] Univ Louisville, Dept Biochem & Mol Biol, Louisville, KY 40202 USA ^[3] Univ Louisville, Dept Ophthalmol & Visual Sci, Louisville, KY 40202 USA ^[4] Louis Stokes Cleveland VA Med Ctr, Cleveland, OH 44106 USA ^[5]

发布时间 2017-04-15

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Human Molecular Genetics

2015年24卷21期

6229-6239页

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Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness

Human Molecular Genetics

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Human Molecular Genetics

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Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness

Human Molecular Genetics

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Human Molecular Genetics

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