Low apolipoprotein A-I levels in Friedreich’s ataxia and in frataxin-deficient cells: Implications for therapy

Friedreich’s ataxia (FA) is an autosomal recessive neurodegenerative disorder, which results primarily from reduced expression of the mitochondrial protein frataxin. FA has an estimated prevalence of one in 50,000 in the population, making it the most common hereditary ataxia. Paradoxically, mortali...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:PLoS One
Päätekijät: Wang, QingQing, Guo, Lili, Strawser, Cassandra J., Hauser, Lauren A., Hwang, Wei-Ting, Snyder, Nathaniel W., Lynch, David R., Mesaros, Clementina, Blair, Ian A.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2018
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5813973/
https://ncbi.nlm.nih.gov/pubmed/29447225
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0192779
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