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Electrocardiographic features of children with Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is a clinically common X-linked recessive myopathy, which is caused by mutation of the gene encoding dystrophin on chromosome Xp21. The onset of heart injury in children with DMD is inconspicuous, and the prognosis is poor once it develops to the stage of heart fail...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9392256/ https://www.ncbi.nlm.nih.gov/pubmed/35987773 http://dx.doi.org/10.1186/s13023-022-02473-9 |