Design of RNAi hairpins for mutation-specific silencing of ataxin-7 and correction of a SCA7 phenotype.

Spinocerebellar ataxia type 7 is a polyglutamine disorder caused by an expanded CAG repeat mutation that results in neurodegeneration. Since no treatment exists for this chronic disease, novel therapies such post-transcriptional RNA interference-based gene silencing are under investigation, in parti...

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Bibliographic Details
Main Authors: Scholefield, J, Greenberg, L, Weinberg, MS, Arbuthnot, P, Abdelgany, A, Wood, M
Format: Journal article
Language:English
Published: 2009