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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...

詳細記述

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書誌詳細
出版年:J Clin Med
主要な著者: Legrand, Lise, Maupain, Carole, Monin, Marie-Lorraine, Ewenczyk, Claire, Isnard, Richard, Alkouri, Rana, Durr, Alexandra, Pousset, Francoise
フォーマット: Artigo
言語:Inglês
出版事項: MDPI 2020
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7356582/
https://ncbi.nlm.nih.gov/pubmed/32481586
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9061630
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