The DOI matches its Crossref record; 150 of the 150 references it cites were found in a registry or an index.
Polyglutamine spinocerebellar ataxias — from genes to potential treatments
Open accessAbstract
The dominantly inherited spinocerebellar ataxias (SCAs) are a large and diverse group of neurodegenerative diseases. The most prevalent SCAs (SCA1, SCA2, SCA3, SCA6 and SCA7) are caused by expansion of a glutamine-encoding CAG repeat in the affected gene. These SCAs represent a substantial portion of the polyglutamine neurodegenerative disorders and provide insight into this class of diseases as a whole. Recent years have seen considerable progress in deciphering the clinical, pathological, physiological and molecular aspects of the polyglutamine SCAs, with these advances establishing a solid base from which to pursue potential therapeutic approaches.
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Hallmarks of neurodegenerative diseases
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Purinergic Receptors in Neurological Diseases With Motor Symptoms: Targets for Therapy
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Metadata
- Authors
- Paulson, H. L., Shakkottai, V. G., Clark, H. B., & Orr, H. T.
- Venue
- Nature Reviews Neuroscience
- Published
- 2017-08-17
- Volume
- 18
- Issue
- 10
- Pages
- 613-626
- ISSN
- 1471-003X (ISSN-L)
- 1471-0048
- OpenAlex
- W2747198643
- Cited by
- 373
- References
- 150
- FWCI
- 3.42
- Type
- journal article
- Language
- en
- Open access
- green
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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