Bidirectional expression of the SCA8 expansion mutation: One mutation, two genes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
http://link.springer.com/content/pdf/10.1007/s12311-008-0010-7.pdf
Reference41 articles.
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3. Schalling M, Hudson T, Buetow K, Housman D. Direct detection of novel expanded trinucleotide repeats in the human genome. Nat Genet. 1993;4:135–9.
4. Koob MD, Moseley ML, Schut LJ, Benzow KA, Bird TD, Day JW, et al. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8). Nat Genet. 1999;21:379–84.
5. Mosemiller AK, Dalton JC, Day JW, Ranum LPW. Molecular genetics of spinocerebellar ataxia type 8 (SCA8). Cytogenet Genome Res. 2003;100:175–83.
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