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Epigenetics in Friedreich's Ataxia: Challenges and Opportunities for Therapy
Friedreich's ataxia (FRDA) is an autosomal recessive neurodegenerative disorder caused by homozygous expansion of a GAA·TTC trinucleotide repeat within the first intron of the FXN gene, leading to reduced FXN transcription and decreased levels of frataxin protein. Recent advances in FRDA resear...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Hindawi Publishing Corporation
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3590757/ https://ncbi.nlm.nih.gov/pubmed/23533785 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/852080 |
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