Friedreich Ataxia: From GAA Triplet–Repeat Expansion to Frataxin Deficiency
- 1 July 2001
- journal article
- review article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 69 (1) , 15-24
- https://doi.org/10.1086/321283
Abstract
No abstract availableThis publication has 72 references indexed in Scilit:
- The mitochondrial proteins Ssq1 and Jac1 are required for the assembly of iron sulfur clusters in mitochondriaJournal of Molecular Biology, 2001
- Unexpected formation of parallel duplex in GAA and TTC trinucleotide repeats of Friedreich’s ataxiaJournal of Molecular Biology, 2000
- dfh is a Drosophila homolog of the Friedreich's ataxia disease geneGene, 2000
- The ferritins: molecular properties, iron storage function and cellular regulationPublished by Elsevier ,1999
- The high-resolution structure of the triplex formed by the GAA/TTC triplet repeat associated with Friedreich’s ataxia 1 1Edited by I. TinocoJournal of Molecular Biology, 1999
- Respiratory deficiency due to loss of mitochondrial DNA in yeast lacking the frataxin homologueNature Genetics, 1997
- Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxinNature Genetics, 1997
- Association of ferrochelatase with Complex I in bovine heart mitochondriaBiochimica et Biophysica Acta (BBA) - General Subjects, 1986
- Free manganese(II) and iron(II) cations can act as intracellular cell controlsFEBS Letters, 1982
- Superoxide‐dependent formation of hydroxyl radicals in the presence of iron saltsFEBS Letters, 1978