Automatic Text-Mining Approach to Identify Molecular Target Candidates Associated with Metabolic Processes for Myotonic Dystrophy Type 1

Myotonic dystrophy type 1 (DM1) is an autosomal dominant hereditary disease caused by abnormal expansion of unstable CTG repeats in the 3′ untranslated region of the myotonic dystrophy protein kinase (DMPK) gene. This disease mainly affects skeletal muscle, resulting in myotonia, progressive distal...

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Detalles Bibliográficos
Autores principales: Kuntawala, Dhvani H., Martins, Filipa, Vitorino, Rui, Rebelo, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9915907/
https://www.ncbi.nlm.nih.gov/pubmed/36767649
http://dx.doi.org/10.3390/ijerph20032283

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9915907/
https://www.ncbi.nlm.nih.gov/pubmed/36767649
http://dx.doi.org/10.3390/ijerph20032283

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