Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patients.
Friedreich ataxia (FRDA) is the most frequent progressive autosomal recessive disorder associated with unstable expansion of GAA trinucleotide repeats in the first intron of the FXN gene, which encodes for the mitochondrial frataxin protein. The number of repeats correlates with disease severity, wh...
Guardado en:
Autores principales: | Mohammad Hossein Salehi, Behnam Kamalidehghan, Massoud Houshmand, Goh Yong Meng, Majid Sadeghizadeh, Omid Aryani, Shahriar Nafissi |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2014
|
Materias: | |
Acceso en línea: | https://doaj.org/article/43abd8be03ab4fa1bbaaedeadcd6407d |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Friedreichs ataxia in a diabetic patient
por: Inna Igorevna Klefortova, et al.
Publicado: (2010) -
Current and emerging treatment options in the management of Friedreich ataxia
por: Michelangelo Mancuso, et al.
Publicado: (2010) -
Epigenetic Heterogeneity in Friedreich Ataxia Underlies Variable FXN Reactivation
por: Layne N. Rodden, et al.
Publicado: (2021) -
PGC-1alpha down-regulation affects the antioxidant response in Friedreich's ataxia.
por: Daniele Marmolino, et al.
Publicado: (2010) -
Digital endpoints for self‐administered home‐based functional assessment in pediatric Friedreich’s ataxia
por: Arne Mueller, et al.
Publicado: (2021)