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Familial cardiolaminopathy due to a previously undescribed LMNA gene mutation
FUNDING ACKNOWLEDGEMENTS: Type of funding sources: None. INTRODUCTION: Cardiolaminopathies are rare genetic alterations, which present diverse mechanical and electrical alterations. OBJECTIVE: To present a family carrying an LMNA gene mutation that although not described manifest clinical and electr...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207693/ http://dx.doi.org/10.1093/europace/euad122.605 |