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A combined voxel-based morphometry and (1)H-MRS study in patients with Friedreich's ataxia.

Friedreich's ataxia (FA) is the most frequent autosomal recessive ataxia and essentially considered a disease of the dorsal root ganglia and spinal cord. It is caused by homozygous GAA expansions in the Frataxin gene in most cases. Although only a few studies have addressed cerebral involvement in FA, cognitive symptoms have lately been emphasized.

Read More: A combined voxel-based morphometry and (1)H-MRS study in patients with Friedreich's ataxia.

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