Excessive rest time during active phase is reliably detected in a mouse model of myotonic dystrophy type 1 using home cage monitoring

Myotonic dystrophy type 1 (DM1) is a dominantly inherited neuromuscular disease caused by the abnormal expansion of CTG-repeats in the 3′-untranslated region of the Dystrophia Myotonica Protein Kinase (DMPK) gene, characterized by multisystemic symptoms including muscle weakness, myotonia, cardio-re...

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Detalles Bibliográficos
Autores principales: Golini, Elisabetta, Rigamonti, Mara, Raspa, Marcello, Scavizzi, Ferdinando, Falcone, Germana, Gourdon, Genevieve, Mandillo, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017452/
https://www.ncbi.nlm.nih.gov/pubmed/36935893
http://dx.doi.org/10.3389/fnbeh.2023.1130055

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017452/
https://www.ncbi.nlm.nih.gov/pubmed/36935893
http://dx.doi.org/10.3389/fnbeh.2023.1130055

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