Iron Metabolism and Mitochondrial Abnormalities in Friedreich Ataxia
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference61 articles.
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3. Friedreich ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion;Campuzano;Science,1996
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5. Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin;Koutnikova;Nat. Genet.,1997
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