Nuclear Envelope Alterations in Myotonic Dystrophy Type 1 Patient-Derived Fibroblasts

Myotonic dystrophy type 1 (DM1) is a hereditary and multisystemic disease characterized by myotonia, progressive distal muscle weakness and atrophy. The molecular mechanisms underlying this disease are still poorly characterized, although there are some hypotheses that envisage to explain the multis...

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Detalles Bibliográficos
Autores principales: Viegas, Diana, Pereira, Cátia D., Martins, Filipa, Mateus, Tiago, da Cruz e Silva, Odete A. B., Herdeiro, Maria Teresa, Rebelo, Sandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745202/
https://www.ncbi.nlm.nih.gov/pubmed/35008948
http://dx.doi.org/10.3390/ijms23010522

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745202/
https://www.ncbi.nlm.nih.gov/pubmed/35008948
http://dx.doi.org/10.3390/ijms23010522

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