A Novel Duplication in ATXN2 as Modifier for Spinocerebellar Ataxia 3 ( SCA3 ) and C9ORF72‐ALS
Author:
Affiliation:
1. Department of Clinical Neuroscience (CNS), Neuro Svenningsson, J5:20 Bioclinicum Karolinska Universitetssjukhuset Stockholm Sweden
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.28334
Reference22 articles.
1. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
2. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
3. Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
4. Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles
5. Age at onset prediction in spinocerebellar ataxia type 3 changes according to population of origin
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