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Skeletal myopathy in a family with lamin A/C cardiac disease
BACKGROUND: The objective of this study was to evaluate patients with known hereditary cardiac conduction and myocardial disease (HCCMD) caused by a lamin A/C gene mutation for skeletal muscle involvement using magnetic resonance imaging (MRI) computed tomography (CT). METHODS: Twenty-one patients w...
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| Publicado no: | Cardiovasc Diagn Ther |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AME Publishing Company
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5059398/ https://ncbi.nlm.nih.gov/pubmed/27747164 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/cdt.2016.03.10 |
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