A new cellular model to follow Friedreich's ataxia development in a time-resolved way

Friedreich's ataxia (FRDA) is a recessive autosomal ataxia caused by reduced levels of frataxin (FXN), an essential mitochondrial protein that is highly conserved from bacteria to primates. The exact role of frataxin and its primary function remain unclear although this information would be ver...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Tommaso Vannocci (Autor), Nathalie Faggianelli (Autor), Silvia Zaccagnino (Autor), Ilaria della Rosa (Autor), Salvatore Adinolfi (Autor), Annalisa Pastore (Autor)
Formato: Libro
Publicado: The Company of Biologists, 2015-07-01T00:00:00Z.
Materias:
Acceso en línea:Connect to this object online.
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!

Internet

Connect to this object online.

3rd Floor Main Library

Detalle de Existencias desde 3rd Floor Main Library
Número de Clasificación: A1234.567
Copia 1 Disponible