## Abstract Friedreich's ataxia (FA) is the most common form of autosomal recessive spinocerebellar ataxia and is often associated with a cardiomyopathy. The disease is caused by an expanded intronic GAA repeat, which results in deficiency of a mitochondrial protein called __frataxin__. In the yeas
Near infrared muscle spectroscopy in patients with Friedreich's ataxia
β Scribed by David R. Lynch; Gwen Lech; Jennifer M. Farmer; Laura J. Balcer; William Bank; Britton Chance; Robert B. Wilson
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 243 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0148-639X
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