Lesion distribution and substrate of white matter damage in myotonic dystrophy type 1: Comparison with multiple sclerosis

Myotonic Dystrophy type 1 (DM1) is an autosomal dominant condition caused by expansion of the CTG triplet repeats within the myotonic dystrophy protein of the kinase (DMPK) gene. The central nervous system is involved in the disease, with multiple symptoms including cognitive impairment. A typical f...

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Detalles Bibliográficos
Autores principales: Leddy, Sara, Serra, Laura, Esposito, Davide, Vizzotto, Camilla, Giulietti, Giovanni, Silvestri, Gabriella, Petrucci, Antonio, Meola, Giovanni, Lopiano, Leonardo, Cercignani, Mara, Bozzali, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848627/
https://www.ncbi.nlm.nih.gov/pubmed/33516936
http://dx.doi.org/10.1016/j.nicl.2021.102562

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848627/
https://www.ncbi.nlm.nih.gov/pubmed/33516936
http://dx.doi.org/10.1016/j.nicl.2021.102562

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