Six Serum miRNAs Fail to Validate as Myotonic Dystrophy Type 1 Biomarkers

Myotonic dystrophy type 1 (DM1) is an autosomal dominant genetic disease caused by expansion of a CTG microsatellite in the 3’ untranslated region of the DMPK gene. Despite characteristic muscular, cardiac, and neuropsychological symptoms, CTG trinucleotide repeats are unstable both in the somatic a...

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Detalles Bibliográficos
Autores principales: Fernandez-Costa, Juan M., Llamusi, Beatriz, Bargiela, Ariadna, Zulaica, Miren, Alvarez-Abril, M. Carmen, Perez-Alonso, Manuel, Lopez de Munain, Adolfo, Lopez-Castel, Arturo, Artero, Ruben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769077/
https://www.ncbi.nlm.nih.gov/pubmed/26919350
http://dx.doi.org/10.1371/journal.pone.0150501

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4769077/
https://www.ncbi.nlm.nih.gov/pubmed/26919350
http://dx.doi.org/10.1371/journal.pone.0150501

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