Significance of NT-proBNP and High-Sensitivity Troponin in Friedreich Ataxia

Background: Friedreich’s ataxia (FA) is a rare autosomal recessive mitochondrial disease resulting of a triplet repeat expansion guanine-adenine-adenine (GAA) in the frataxin (FXN) gene, exhibiting progressive cerebellar ataxia, diabetes and cardiomyopathy. We aimed to determine the relationship bet...

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Detalles Bibliográficos
Autores principales: Legrand, Lise, Maupain, Carole, Monin, Marie-Lorraine, Ewenczyk, Claire, Isnard, Richard, Alkouri, Rana, Durr, Alexandra, Pousset, Francoise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356582/
https://www.ncbi.nlm.nih.gov/pubmed/32481586
http://dx.doi.org/10.3390/jcm9061630

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356582/
https://www.ncbi.nlm.nih.gov/pubmed/32481586
http://dx.doi.org/10.3390/jcm9061630

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