Interruptions in the Expanded ATTCT Repeat of Spinocerebellar Ataxia Type 10: Repeat Purity as a Disease Modifier?
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics
Reference21 articles.
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2. Evolution of the Freidreich’s ataxia trinucleotide repeat expansion: founder effect and premutations;Cossee;Proc Natl Acad Sci USA,1997
3. Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10;Grewal;Arch Neurol,2002
4. Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia;Grewal;Neurology,1998
5. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1;Gunter;Hum Mol Genet,1998
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