SCA8 repeat expansion coexists with SCA1--not only with SCA6.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

11 citing papers in PubMed.

1. A Novel Co-existence of Spinocerebellar Ataxia 1 and Spinocerebellar Ataxia 2 Mutations in Indian Patients.Movement disorders clinical practice · 2022
   Article
2. Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool.Advanced genetics (Hoboken, N.J.) · 2022
   Article
3. The First Case of Spinocerebellar Ataxia Type 8 in Monozygotic Twins.Internal medicine (Tokyo, Japan) · 2020
   Article
4. SCA8 should not be tested in isolation for ataxia.Neurology. Genetics · 2017
   Article
5. Bolivian kindred with combined spinocerebellar ataxia types 2 and 10.Acta neurologica Scandinavica · 2015
   Article
6. Spinocerebellar Ataxia 2 and 12 Mutations in an Indian Family with Cerebellar Ataxia and Slow Saccades.Movement disorders clinical practice · 2014
   Article
7. Non-Ataxic Phenotypes of SCA8 Mimicking Amyotrophic Lateral Sclerosis and Parkinson Disease.Journal of clinical neurology (Seoul, Korea) · 2013
   Article
8. RNA-mediated toxicity in neurodegenerative disease.Molecular and cellular neurosciences · 2013
   Review
9. Bidirectional expression of the SCA8 expansion mutation: one mutation, two genes.Cerebellum (London, England) · 2008
   Article
10. Genetic and molecular aspects of spinocerebellar ataxias.Neuropsychiatric disease and treatment · 2005
    Article
11. A Case of Two Repeats: Huntington's Disease and Spinocerebellar Ataxia Type 8.Movement disorders clinical practice
    Article

Corrections and comments

• Comment on
  SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6.2003

Authors and funding

4 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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