Identification of telomere dysfunction in Friedreich ataxia

BACKGROUND: Friedreich ataxia (FRDA) is a progressive inherited neurodegenerative disorder caused by mutation of the FXN gene, resulting in decreased frataxin expression, mitochondrial dysfunction and oxidative stress. A recent study has identified shorter telomeres in FRDA patient leukocytes as a p...

Descripción completa

Detalles Bibliográficos
Autores principales: Anjomani Virmouni, Sara, Al-Mahdawi, Sahar, Sandi, Chiranjeevi, Yasaei, Hemad, Giunti, Paola, Slijepcevic, Predrag, Pook, Mark A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462004/
https://www.ncbi.nlm.nih.gov/pubmed/26059974
http://dx.doi.org/10.1186/s13024-015-0019-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462004/
https://www.ncbi.nlm.nih.gov/pubmed/26059974
http://dx.doi.org/10.1186/s13024-015-0019-6

Ejemplares similares