ArticleAmerican journal of human genetics1997
Linkage disequilibrium between the spinocerebellar ataxia 3/Machado-Joseph disease mutation and two intragenic polymorphisms, one of which, X359Y, affects the stop codon.
Article in American journal of human genetics, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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Who cites it
7 citing papers in PubMed.
- Role of Repeat Tract Structure and the rs7158733 SNP in Spinocerebellar Ataxia 3.International journal of molecular sciences · 2025Article
- Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3.Science translational medicine · 2020Article
- Population genetics and new insight into range of CAG repeats of spinocerebellar ataxia type 3 in the Han Chinese population.PloS one · 2015Article
- Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics.Orphanet journal of rare diseases · 2013Review
- High frequency of Machado-Joseph disease identified in southeastern Chinese kindreds with spinocerebellar ataxia.BMC medical genetics · 2010Article
- Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.American journal of human genetics · 2001Article
- An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients.Brain pathology (Zurich, Switzerland) · 1998Article
Corrections and comments
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Authors and funding
10 authors.
Funding
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Abstract
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Registered trials
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