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Genome-Wide Screen for Modifiers of Ataxin-3 Neurodegeneration in Drosophila

Spinocerebellar ataxia type-3 (SCA3) is among the most common dominantly inherited ataxias, and is one of nine devastating human neurodegenerative diseases caused by the expansion of a CAG repeat encoding glutamine within the gene. The polyglutamine domain confers toxicity on the protein Ataxin-3 le...

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Bibliografiske detaljer
Main Authors: Bilen, Julide, Bonini, Nancy M
Format: Artigo
Sprog:Inglês
Udgivet: Public Library of Science 2007
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2041992/
https://ncbi.nlm.nih.gov/pubmed/17953484
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.0030177
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