Long intronic GAA•TTC repeats induce epigenetic changes and reporter gene silencing in a molecular model of Friedreich ataxia
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics
Link
http://academic.oup.com/nar/article-pdf/36/19/6056/16748728/gkn604.pdf
Reference69 articles.
1. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion;Campuzano;Science,1996
2. Friedreich's ataxia.;Pandolfo,2006
3. Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations;Cossee;Proc. Natl Acad. Sci. USA,1997
4. The Friedreich ataxia GAA triplet repeat: premutation and normal alleles;Montermini;Hum. Mol. Genet.,1997
5. Iron metabolism and mitochondrial abnormalities in Friedreich ataxia;Pandolfo;Blood Cells Mol. Dis.,2002
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