Treatment of dilated cardiomyopathy in a mouse model of Friedreich’s ataxia using N-acetylcysteine and identification of alterations in microRNA expression that could be involved in its pathogenesis
Author:
Funder
National Health and Medical Research Council of Australia
Muscular Dystrophy Association
Publisher
Elsevier BV
Subject
Pharmacology
Reference112 articles.
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2. Friedreich ataxia: molecular mechanisms, redox considerations, and therapeutic opportunities;Santos;Antioxid. Redox Signal.,2010
3. The heart in Friedreich’s ataxia: basic findings and clinical implications;Payne;Prog. Pediatr. Cardiol.,2011
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