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Campuzano V, Montermini L, Molt\u00f2 MD, et al. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 271: 1423-1427, 1996.","DOI":"10.1126\/science.271.5254.1423"},{"key":"2","unstructured":"2. Pandolfo M. Friedreich ataxia: the clinical picture. J Neurol 256 (Suppl 1): 3-8, 2009."},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Delatycki MB, Knight M, Koenig M, Cossee M, Williamson R, Forrest SM. G130V, a common FRDA point mutation, appears to have arisen from a common founder. Hum Genet 105: 343-346, 1999.","DOI":"10.1007\/s004399900142"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Labuda M, Labuda D, Miranda C, et al. Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion. Neurology 54: 2322-2324, 2000.","DOI":"10.1212\/WNL.54.12.2322"},{"key":"5","doi-asserted-by":"publisher","unstructured":"5. Harding AE. 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Singh I, Faruq M, Mukherjee O, et al. North and South Indian populations share a common ancestral origin of Friedreich's ataxia but vary in age of GAA repeat expansion. Ann Hum Genet 74: 202-210, 2010.","DOI":"10.1111\/j.1469-1809.2010.00569.x"},{"key":"13","unstructured":"13. Cossee M, Schmitt M, Campuzano V, et al. Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations. Proc Natl Acad Sci U S A 94: 7452-7457, 1997."},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Monros E, Molto MD, Martinez F, et al. Phenotype correlation and intergenerational dynamics of the Friedreich ataxia GAA trinucleotide repeat. Am J Hum Genet 61: 101-110, 1997.","DOI":"10.1086\/513887"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Mukerji M, Choudhry S, Saleem Q, Padma MV, Maheshwari MC, Jain S. Molecular analysis of Friedreich's ataxia locus in the Indian population. 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