The Dysferlin Transcript Containing the Alternative Exon 40a is Essential for Myocyte Functions

Dysferlinopathies are a group of muscular dystrophies caused by recessive mutations in the DYSF gene encoding the dysferlin protein. Dysferlin is a transmembrane protein involved in several muscle functions like T-tubule maintenance and membrane repair. In 2009, a study showed the existence of fourt...

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Detalles Bibliográficos
Autores principales: Ballouhey, Océane, Courrier, Sébastien, Kergourlay, Virginie, Gorokhova, Svetlana, Cerino, Mathieu, Krahn, Martin, Lévy, Nicolas, Bartoli, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650162/
https://www.ncbi.nlm.nih.gov/pubmed/34888307
http://dx.doi.org/10.3389/fcell.2021.754555

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650162/
https://www.ncbi.nlm.nih.gov/pubmed/34888307
http://dx.doi.org/10.3389/fcell.2021.754555

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