Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph disease
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference27 articles.
1. Gametic and somatic tissue–specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1
2. Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I
3. Analysis of the SCAI CAG repeat in a large number of families with dominant ataxia: Clinical and molecular correlations
4. Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity
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1. The S-Factor, a New Measure of Disease Severity in Spinocerebellar Ataxia: Findings and Implications;The Cerebellum;2022-08-12
2. Tissue-specific and repeat length-dependent somatic instability of the X-linked dystonia parkinsonism-associated CCCTCT repeat;Acta Neuropathologica Communications;2022-04-08
3. Current and emerging treatment modalities for spinocerebellar ataxias;Expert Review of Neurotherapeutics;2022-02-01
4. Tissue-specific and repeat length-dependent somatic instability of the X-linked dystonia parkinsonism-associated CCCTCT repeat;2022-01-28
5. Mutant Ataxin-3–Containing Aggregates (MATAGGs) in Spinocerebellar Ataxia Type 3: Dynamics of the Disorder;Molecular Neurobiology;2021-02-24
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