Protein Phosphorylation Alterations in Myotonic Dystrophy Type 1: A Systematic Review

Among the most common muscular dystrophies in adults is Myotonic Dystrophy type 1 (DM1), an autosomal dominant disorder characterized by myotonia, muscle wasting and weakness, and multisystemic dysfunctions. This disorder is caused by an abnormal expansion of the CTG triplet at the DMPK gene that, w...

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Detalles Bibliográficos
Autores principales: Costa, Adriana, Cruz, Ana C., Martins, Filipa, Rebelo, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9965115/
https://www.ncbi.nlm.nih.gov/pubmed/36834509
http://dx.doi.org/10.3390/ijms24043091

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9965115/
https://www.ncbi.nlm.nih.gov/pubmed/36834509
http://dx.doi.org/10.3390/ijms24043091

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