Metabolic Alterations in Myotonic Dystrophy Type 1 and Their Correlation with Lipin

Myotonic dystrophy type 1 (DM1) is an autosomal dominant hereditary and multisystemic disease, characterized by progressive distal muscle weakness and myotonia. Despite huge efforts, the pathophysiological mechanisms underlying DM1 remain elusive. In this review, the metabolic alterations observed i...

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Detalles Bibliográficos
Autores principales: Mateus, Tiago, Martins, Filipa, Nunes, Alexandra, Herdeiro, Maria Teresa, Rebelo, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918590/
https://www.ncbi.nlm.nih.gov/pubmed/33673200
http://dx.doi.org/10.3390/ijerph18041794

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918590/
https://www.ncbi.nlm.nih.gov/pubmed/33673200
http://dx.doi.org/10.3390/ijerph18041794

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