Spinocerebellar Ataxia 2 (SCA2)
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Elsevier
Reference83 articles.
1. Clinical and molecular analysis of a pedigree of southern Italian ancestry with spinocerebellar ataxia type 2;Adams;Neurology,1997
2. Autosomal dominant cerebellar ataxia type I, Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3;Abele;Brain,1997
3. Identification of alternative splicing of spinocerebellar ataxia type 2 gene;Affaitati;Gene,2001
4. Spinocerebellar ataxia type 2 (SCA2) in an infant with extreme CAG repeat expansion;Babovic-Vuksanovic;Am. J. Med. Genet.,1998
5. Autosomal dominant cerebellar ataxia type 1: clinical features and MRI in families with SCA1, SCA2 and SCA3;Burk;Brain,1996
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset;Brain;2005-07-06
2. Hprt(CAG)146 mice: Age of onset of behavioral abnormalities, time course of neuronal intranuclear inclusion accumulation, neurotransmitter marker alterations, mitochondrial function markers, and susceptibility to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine;The Journal of Comparative Neurology;2003-08-25
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