Baroreflex sensitivity in facioscapulohumeral muscular dystrophy

Facioscapulohumeral muscular dystrophy (FSHD), a common form of muscular dystrophy, is caused by a genetic mutation that alters DUX4 gene expression. This mutation contributes to significant skeletal muscle loss. Although it is suggested that cardiac muscle may be spared, people with FSHD have demon...

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Detalles Bibliográficos
Autores principales: Anselmo, Miguel, Coffman, Shandon, Larson, Mia, Vera, Kathryn, Lee, Emma, McConville, Mary, Kyba, Michael, Keller‐Ross, Manda L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023871/
https://www.ncbi.nlm.nih.gov/pubmed/35451178
http://dx.doi.org/10.14814/phy2.15277

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023871/
https://www.ncbi.nlm.nih.gov/pubmed/35451178
http://dx.doi.org/10.14814/phy2.15277

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