Frataxin knockdown in human astrocytes triggers cell death and the release of factors that cause neuronal toxicity
Friedreich's ataxia (FA) is a recessive, predominantly neurodegenerative disorder caused in most cases by mutations in the first intron of the frataxin (FXN) gene. This mutation drives the expansion of a homozygous GAA repeat that results in decreased levels of FXN transcription and frataxin pr...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2015-04-01
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Series: | Neurobiology of Disease |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S096999611400388X |