Author:
Milne Sarah C.,Hocking Darren R.,Georgiou-Karistianis Nellie,Murphy Anna,Delatycki Martin B.,Corben Louise A.
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Reference59 articles.
1. Cossée M, Schmitt M, Campuzano V, Reutenauer L, Moutou C, Mandel JL, et al. Evolution of the Friedreich’s ataxia trinucleotide repeat expansion: founder effect and premutations. Proc Natl Acad Sci U S A. 1997;94:7452–7.
2. Campuzano V, Montermini L, Moltò MD, Pianese L, Cossée M, Cavalcanti F, et al. Friedreich’s ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science. 1996;271:1423–7.
3. Delatycki MB, Williamson R, Forrest SM. Friedreich ataxia: an overview. J Med Genet. 2000;37:1–8.
4. Bidichandani SI, Delatycki MB. Friedreich ataxia. In GeneReviews. University of Washington. 1993. http://www.ncbi.nlm.nih.gov/books/NBK1281 . Accessed 10 Sept 2013.
5. Pandolfo M. Friedreich ataxia: the clinical picture. J Neurol. 2009;256 Suppl 1:3–8.