Transcriptome Analysis in a Primary Human Muscle Cell Differentiation Model for Myotonic Dystrophy Type 1

Myotonic dystrophy type 1 (DM1) is caused by CTG-repeat expansions leading to a complex pathology with a multisystemic phenotype that primarily affects the muscles and brain. Despite a multitude of information, especially on the alternative splicing of several genes involved in the pathology, inform...

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Detalles Bibliográficos
Autores principales: Todorow, Vanessa, Hintze, Stefan, Kerr, Alastair R. W., Hehr, Andreas, Schoser, Benedikt, Meinke, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395314/
https://www.ncbi.nlm.nih.gov/pubmed/34445314
http://dx.doi.org/10.3390/ijms22168607

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395314/
https://www.ncbi.nlm.nih.gov/pubmed/34445314
http://dx.doi.org/10.3390/ijms22168607

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