The pathogenesis of Friedreich ataxia and the structure and function of frataxin
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
http://link.springer.com/content/pdf/10.1007/s00415-009-1003-2.pdf
Reference76 articles.
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2. Bradley JL, Blake JC, Chamberlain S,Thomas PK, Cooper JM, Schapira AH(2000) Clinical, biochemical andmolecular genetic correlations inFriedreich’s ataxia. Hum Mol Genet9:275–282
3. Rötig A, de Lonlay P, Chretien D, FouryF, Koenig M, Sidi D, Munnich A, RustinP (1997) Aconitase and mitochondrialiron-sulphur protein deficiency inFriedreich ataxia. Nat Genet 17:215–217
4. Martelli A, Wattenhofer-Donzé M,Schmucker S, Bouvet S, Reutenauer L,Puccio H (2007) Frataxin is essentialfor extramitochondrial Fe-S clusterproteins in mammalian tissues. HumMol Genet 16:2651–2658
5. Radisky DC, Babcock MC, Kaplan J(1999) The yeast frataxin homologuemediates mitochondrial iron efflux:evidence for a mitochondrial ironcycle. J Biol Chem 274:4497–4499
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