Rescue of amyotrophic lateral sclerosis phenotype in a mouse model by intravenous AAV9‐ADAR2 delivery to motor neurons

Abstract Amyotrophic lateral sclerosis (ALS) is the most common adult‐onset motor neuron disease, and the lack of effective therapy results in inevitable death within a few years of onset. Failure of GluA2 RNA editing resulting from downregulation of the RNA‐editing enzyme adenosine deaminase acting...

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Bibliographic Details
Main Authors: Takenari Yamashita, Hui Lin Chai, Sayaka Teramoto, Shoji Tsuji, Kuniko Shimazaki, Shin‐ichi Muramatsu, Shin Kwak
Format: Article
Language:English
Published: Springer Nature 2013-09-01
Series:EMBO Molecular Medicine
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Online Access:https://doi.org/10.1002/emmm.201302935
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