Myofibre Hyper-Contractility in Horses Expressing the Myosin Heavy Chain Myopathy Mutation, MYH1(E321G)

Myosinopathies are defined as a group of muscle disorders characterized by mutations in genes encoding myosin heavy chains. Their exact molecular and cellular mechanisms remain unclear. In the present study, we have focused our attention on a MYH1-related E321G amino acid substitution within the hea...

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Detalles Bibliográficos
Autores principales: Ochala, Julien, Finno, Carrie J., Valberg, Stephanie J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699922/
https://www.ncbi.nlm.nih.gov/pubmed/34943936
http://dx.doi.org/10.3390/cells10123428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8699922/
https://www.ncbi.nlm.nih.gov/pubmed/34943936
http://dx.doi.org/10.3390/cells10123428

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