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Cardiac Involvement and Arrhythmias Associated with Myotonic Dystrophy
Myotonic dystrophy is an autosomal dominant genetic disease of nucleotide expansion resulting in neuromuscular disease with two distinct subtypes. There are significant systemic manifestations of this condition including progressive muscular decline, neurologic abnormalities, and cardiac disease. Gi...
Autores principales: | McBride, Daniel, Deshmukh, Amrish, Shore, Supriya, Elafros, Melissa A., Liang, Jackson J. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9518819/ https://www.ncbi.nlm.nih.gov/pubmed/36177340 http://dx.doi.org/10.31083/j.rcm2304126 |
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