Cargando…
Selected missense mutations impair frataxin processing in Friedreich ataxia
Formato: | Online Artículo Texto |
---|---|
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5634344/ https://www.ncbi.nlm.nih.gov/pubmed/29046887 http://dx.doi.org/10.1002/acn3.490 |
Ejemplares similares
-
Selected missense mutations impair frataxin processing in Friedreich ataxia
por: Clark, Elisia, et al.
Publicado: (2017) -
The First Cellular Models Based on Frataxin Missense Mutations That Reproduce Spontaneously the Defects Associated with Friedreich Ataxia
por: Calmels, Nadège, et al.
Publicado: (2009) -
Frataxin levels in peripheral tissue in Friedreich ataxia
por: Lazaropoulos, Michael, et al.
Publicado: (2015) -
Novel Point Mutations in Frataxin Gene in Iranian Patients with Friedreich’s Ataxia
por: HEIDARI, Mohammad Mehdi, et al.
Publicado: (2014) -
Posttranslational regulation of mitochondrial frataxin and identification of compounds that increase frataxin levels in Friedreich’s ataxia
por: Hackett, Peter T., et al.
Publicado: (2022)