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Altered lipid metabolism in a Drosophila model of Friedreich's ataxia

Friedreich's ataxia (FRDA) is the most common form of autosomal recessive ataxia caused by a deficit in the mitochondrial protein frataxin. Although demyelination is a common symptom in FRDA patients, no multicellular model has yet been developed to study the involvement of glial cells in FRDA....

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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: Navarro, Juan A., Ohmann, Elisabeth, Sanchez, Diego, Botella, José A., Liebisch, Gerhard, Moltó, María D., Ganfornina, María D., Schmitz, Gerd, Schneuwly, Stephan
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7108586/
https://ncbi.nlm.nih.gov/pubmed/20460268
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq183
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