Disrupting the Molecular Pathway in Myotonic Dystrophy

Myotonic dystrophy is the most common muscular dystrophy in adults. It consists of two forms: type 1 (DM1) and type 2 (DM2). DM1 is associated with a trinucleotide repeat expansion mutation, which is transcribed but not translated into protein. The mutant RNA remains in the nucleus, which leads to a...

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Detalles Bibliográficos
Autores principales: Xing, Xiaomeng, Kumari, Anjani, Brown, Jake, Brook, John David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8708683/
https://www.ncbi.nlm.nih.gov/pubmed/34948025
http://dx.doi.org/10.3390/ijms222413225

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8708683/
https://www.ncbi.nlm.nih.gov/pubmed/34948025
http://dx.doi.org/10.3390/ijms222413225

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