Deciphering the Complex Molecular Pathogenesis of Myotonic Dystrophy Type 1 through Omics Studies

Omics studies are crucial to improve our understanding of myotonic dystrophy type 1 (DM1), the most common muscular dystrophy in adults. Employing tissue samples and cell lines derived from patients and animal models, omics approaches have revealed the myriad alterations in gene and microRNA express...

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Detalles Bibliográficos
Autores principales: Espinosa-Espinosa, Jorge, González-Barriga, Anchel, López-Castel, Arturo, Artero, Rubén
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836095/
https://www.ncbi.nlm.nih.gov/pubmed/35163365
http://dx.doi.org/10.3390/ijms23031441

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8836095/
https://www.ncbi.nlm.nih.gov/pubmed/35163365
http://dx.doi.org/10.3390/ijms23031441

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