Yet another spinocerebellar ataxia—will it ever end?-Reference-Cited by-同舟云学术

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Yet another spinocerebellar ataxia—will it ever end?

Published:2002-12 Issue:8 Volume:1 Page:471
ISSN:1474-4422
Container-title:The Lancet Neurology
language:en
Short-container-title:The Lancet Neurology

Author:

Paulson Henry

Publisher

Elsevier BV

Subject

Clinical Neurology

Reference3 articles.

1. Ataxia and hereditary disorders;Paulson;Neurel Clin,2001

2. A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1;Vuillaume;Ann Neurol,2002

3. Clinical features and genetic analysis of a new form of spinocerebellar atasia;Devos;Neurology,2001

Cited by 5 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. A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome;Movement Disorders;2014-12-27

2. Autosomal dominant cerebellar ataxias: a systematic review of clinical features;European Journal of Neurology;2014-02-12

3. Clinical Clues to Differentiating Inherited and Noninherited Etiologies of Childhood Ataxias;The Journal of Pediatrics;2012-01

4. Yet another spinocerebellar ataxia: The saga continues;Neurology;2008-08-18

5. Ataxin-10, the Spinocerebellar Ataxia Type 10 Neurodegenerative Disorder Protein, Is Essential for Survival of Cerebellar Neurons;Journal of Biological Chemistry;2004-08

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