Central Nervous System Involvement as Outcome Measure for Clinical Trials Efficacy in Myotonic Dystrophy Type 1

Increasing evidences indicate that in Myotonic Dystrophy type 1 (DM1 or Steinert disease), an autosomal dominant multisystem disorder caused by a (CTG)n expansion in DMPK gene on chromosome 19q13. 3, is the most common form of inherited muscular dystrophy in adult patients with a global prevalence o...

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Detalles Bibliográficos
Autores principales: Simoncini, Costanza, Spadoni, Giulia, Lai, Elisa, Santoni, Lorenza, Angelini, Corrado, Ricci, Giulia, Siciliano, Gabriele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575726/
https://www.ncbi.nlm.nih.gov/pubmed/33117249
http://dx.doi.org/10.3389/fneur.2020.00624

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7575726/
https://www.ncbi.nlm.nih.gov/pubmed/33117249
http://dx.doi.org/10.3389/fneur.2020.00624

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