Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management

Mitochondrial disease refers to a heterogenous group of genetic disorders that result from dysfunction of the final common pathway of energy metabolism. Mitochondrial DNA mutations affect key components of the respiratory chain and account for the majority of mitochondrial disease in adults. Owing t...

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Detalles Bibliográficos
Autores principales: Bates, Matthew G. D., Bourke, John P., Giordano, Carla, d'Amati, Giulia, Turnbull, Douglass M., Taylor, Robert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530901/
https://www.ncbi.nlm.nih.gov/pubmed/22936362
http://dx.doi.org/10.1093/eurheartj/ehs275

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530901/
https://www.ncbi.nlm.nih.gov/pubmed/22936362
http://dx.doi.org/10.1093/eurheartj/ehs275

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