Friedreich's ataxia protein: phylogenetic evidence for mitochondrial dysfunction
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference32 articles.
1. Mitochondrial myopathies: genetic defects
2. The expanding clinical spectrum of mitochondrial diseases
3. A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase
4. Harding, A.E. (1984) The Hereditary Ataxias and Related Disorders, Churchill Livingston
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