The Spinocerebellar Ataxias
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Pharmacology (medical),Neurology (clinical),Pharmacology
Reference87 articles.
1. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
2. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
3. The gene for Machado–Joseph disease maps to human chromosome 14q
4. The gene for Machado–Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q
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1. Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study;Journal of Neurology, Neurosurgery & Psychiatry;2024-02-21
2. Comparison of Cardiac Autonomic Function in Type 2 Spinocerebellar Ataxia With Normal Control Using Heart Rate Variability as a Tool: A Cross-Sectional Study in Eastern India;Cureus;2021-11-30
3. Sphingolipid metabolism governs Purkinje cell patterned degeneration in Atxn1[82Q]/+ mice;P NATL ACAD SCI USA;2021
4. Sphingolipid metabolism governs Purkinje cell patterned degeneration in Atxn1[82Q]/+ mice;Proceedings of the National Academy of Sciences;2021-09-03
5. Genetic Modeling of the Neurodegenerative Disease Spinocerebellar Ataxia Type 1 in Zebrafish;International Journal of Molecular Sciences;2021-07-08
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