CTA/CTG expansions at the SCA 8 locus in multiple system atrophy
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,General Medicine,Surgery
Reference19 articles.
1. Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy;Cellini;Arch Neurol,2001
2. Spinocerebellar ataxia type 8: clinical features in a large family;Day;Neurology,2000
3. High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal alleles;Silveira;Am J Hum Genet,2000
4. SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance;Moseley;Hum Mol Genet,2000
5. SCA8 repeat expansion: large CTA/CTG repeat alleles are more common in ataxic patients, including those with SCA6;Izumi;Am J Hum Genet,2003
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1. Genetic profiles of multiple system atrophy revealed by exome sequencing, long‐read sequencing and spinocerebellar ataxia repeat expansion analysis;European Journal of Neurology;2024-08-17
2. Chinese abnormal compound heterozygote spinocerebellar ataxia type 8: a case report;Neurological Sciences;2022-01-07
3. Gene regulation by antisense transcription: A focus on neurological and cancer diseases;Biomedicine & Pharmacotherapy;2022-01
4. Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy;Clinical Autonomic Research;2021-01-27
5. Genetic and clinical analyses of spinocerebellar ataxia type 8 in mainland China;Journal of Neurology;2019-08-30
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