Spinocerebellar ataxia 2 (SCA2)

Author:

Lastres-Becker Isabel,Rüb Udo,Auburger Georg

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Reference103 articles.

1. Wadia NH, Swami RK. A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families). Brain. 1971;94:359–74.

2. Orozco G, Estrada R, Perry TL, Arana J, Fernandez R, Gonzalez-Quevedo A, et al. Dominantly inherited olivopontocerebellar atrophy from Eastern Cuba: Clinical, neuropathological, and biochemical findings. J Neurol Sci. 1989;93:37–50.

3. Auburger G, Diaz GO, Capote RF, Sanchez SG, Perez MP, del Cueto ME, et al. Autosomal dominant ataxia: Genetic evidence for locus heterogeneity from a Cuban foundereffect population. Am J Hum Genet. 1990;46:1163–77.

4. Orozco Diaz G, Nodarse Fleites A, Cordoves Sagaz R, Auburger G. Autosomal dominant cerebellar ataxia: Clinical analysis of 263 patients from a homogeneous population in Holguin, Cuba. Neurology. 1990;40:1369–75.

5. Velazquez Perez L, Almaguer Mederos L, Santos Falcon N, Hechavarria R, Sanchez Cruz G, Paneque HM. [Spinocerebellar ataxia type 2 in Cuba. A study of the electrophysiological phenotype and its correlation with clinical and molecular variables]. Rev Neurol. 2001;33:1129–36.

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