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Clinical features and progression of cardiomyopathy in patients with Friedreich's ataxia

✍ Scribed by Pureza, Vincent; Hasadsri, Linda; Highsmith, W. Edward; Oglesbee, Devin

Book ID
122328628
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
46 KB
Volume
13
Category
Article
ISSN
1567-7249

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## Abstract Friedreich ataxia is an inherited, progressive, neurodegenerative disorder that is clinically heterogeneous. It is caused by a trinucleotide (GAA) repeat expansion resulting in frataxin loss and oxidative stress. We assessed clinical features including the development of cardiomyopathy