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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...
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| 出版年: | J Clin Med |
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| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
MDPI
2020
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| 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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