Spinocerebellar ataxia type 2 (SCA2) with white matter involvement

Author:

Armstrong J.,Bonaventura I.,Rojo A.,González G.,Corral J.,Nadal N.,Volpini V.,Ferrer I.

Publisher

Elsevier BV

Subject

General Neuroscience

Reference16 articles.

1. Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families;Cancel;Hum. Mol. Genet.,1997

2. CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms;Choudhry;Hum. Mol. Genet.,2001

3. Spinocerebellar ataxia 2 (SCA2): morphometric analysis in 11 autopsies;Estrada;Acta Neuropathol.,1999

4. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia;Geschwind;Am. J. Hum. Genet.,1997

5. Localization of the candidate gene d-amino acid oxidase outside the refined I-cM region of spinocerenellar ataxia 2;Gispert;Am. J. Hum. Genet.,1995

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