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Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes
Cardiomyopathies are mostly determined by genetic mutations affecting either cardiac muscle cell structure or function. Nevertheless, cardiomyopathies may also be part of complex clinical phenotypes in the spectrum of neuromuscular (NMD) or mitochondrial diseases (MD). The aim of this study is to de...
Autores principales: | Monda, Emanuele, Lioncino, Michele, Caiazza, Martina, Simonelli, Vincenzo, Nesti, Claudia, Rubino, Marta, Perna, Alessia, Mauriello, Alfredo, Budillon, Alberta, Pota, Vincenzo, Bruno, Giorgia, Varone, Antonio, Nigro, Vincenzo, Santorelli, Filippo Maria, Pacileo, Giuseppe, Russo, Maria Giovanna, Frisso, Giulia, Sampaolo, Simone, Limongelli, Giuseppe |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218839/ https://www.ncbi.nlm.nih.gov/pubmed/37240454 http://dx.doi.org/10.3390/ijms24109108 |
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