Consequences of Lmna Exon 4 Mutations in Myoblast Function

Laminopathies are causally associated with mutations on the Lamin A/C gene (LMNA). To date, more than 400 mutations in LMNA have been reported in patients. These mutations are widely distributed throughout the entire gene and are associated with a wide range of phenotypes. Unfortunately, little is k...

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Detalles Bibliográficos
Autores principales: Gómez-Domínguez, Déborah, Epifano, Carolina, de Miguel, Fernando, Castaño, Albert García, Vilaplana-Martí, Borja, Martín, Alberto, Amarilla-Quintana, Sandra, Bertrand, Anne T, Bonne, Gisèle, Ramón-Azcón, Javier, Rodríguez-Milla, Miguel A, Pérez de Castro, Ignacio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291140/
https://www.ncbi.nlm.nih.gov/pubmed/32455813
http://dx.doi.org/10.3390/cells9051286

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291140/
https://www.ncbi.nlm.nih.gov/pubmed/32455813
http://dx.doi.org/10.3390/cells9051286

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