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Neurology

Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutations.


PMID 24719489

Abstract

Autosomal recessive ataxias affect about 1 person in 20,000. Friedreich ataxia accounts for one-third of the cases in Caucasians; the others are due to a growing list of very rare molecular defects, including mild forms of metabolic diseases. In nearly 50%, the genetic cause remains undetermined.

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