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Baroreflex sensitivity in facioscapulohumeral muscular dystrophy
Abstract 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 h...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley
2022-04-01
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| Colecção: | Physiological Reports |
| Assuntos: | |
| Acesso em linha: | https://doi.org/10.14814/phy2.15277 |
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