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Description

Moison C, Chagraoui J, Caron MC, Gagn JP, Coulombe Y, Poirier GG, et al

Olive, M.E

Abstract Abnormal iron metabolism, mitochondrial dysfunction and the derived oxidative damage are the main pathogeneses of Friedrich's ataxia (FRDA), a single-gene inherited recessive neurodegenerative disease characterized by progressive cerebellar and sensory ataxia