A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21‐q23
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/126/6/1293/9172040/awg130.pdf
Reference36 articles.
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3. Cottingham RW Jr, Idury RM, Schaffer AA. Faster sequential genetic linkage computations. Am J Hum Genet1993; 53: 252–63.
4. David G, Abbas N, Stevanin G, Dürr A, Yvert G, Cancel G, et al. Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nature Genet1997; 17: 65–70.
5. Devos D, Schraen‐Maschke S, Vuillaume I, Dujardin K, Naze P, Willoteaux C, et al. Clinical features and genetic analysis of a new form of spinocerebellar ataxia. Neurology2001; 56: 234–8.
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