Small RNA-seq analysis of circulating miRNAs to identify phenotypic variability in Friedreich’s ataxia patients

Friedreich’s ataxia (FRDA; OMIM 229300), an autosomal recessive neurodegenerative mitochondrial disease, is the most prevalent hereditary ataxia. In addition, FRDA patients have shown additional non-neurological features such as scoliosis, diabetes, and cardiac complications. Hypertrophic cardiomyop...

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Detalles Bibliográficos
Autores principales: Seco-Cervera, Marta, González-Rodríguez, Dayme, Ibáñez-Cabellos, José Santiago, Peiró-Chova, Lorena, Pallardó, Federico V, García-Giménez, José Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Data Descriptor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839159/
https://www.ncbi.nlm.nih.gov/pubmed/29509186
http://dx.doi.org/10.1038/sdata.2018.21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839159/
https://www.ncbi.nlm.nih.gov/pubmed/29509186
http://dx.doi.org/10.1038/sdata.2018.21

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