AAV1/2-mediated BDNF gene therapy in a transgenic rat model of Huntington’s disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
http://www.nature.com/articles/gt2015113.pdf
Reference49 articles.
1. Ross CA, Tabrizi SJ . Huntington’s disease: from molecular pathogenesis to clinical treatment. Lancet Neurol 2011; 10: 83–98.
2. Walker FO . Huntington's disease. Lancet 2007; 369: 218–228.
3. The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington’s disease chromosomes. Cell 1993; 72: 971–983.
4. Zuccato C, Valenza M, Cattaneo E . Molecular mechanisms and potential therapeutical targets in Huntington's disease. Physiol Rev 2010; 90: 905–981.
5. Vonsattel JP, Keller C, Del Pilar Amaya M . Neuropathology of Huntington’s disease. Handb Clin Neurology 2008; 89: 599–618.
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