Spinocerebellar ataxia type 17 repeat in patients with Huntington's disease-like and ataxia
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Reference5 articles.
1. SCA17 homozygote showing Huntington's disease-like phenotype
2. Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes
3. Spinocerebellar ataxia type 17 in the Yugoslav population
4. Trinucleotide Repeats in 202 Families With Ataxia
5. Phenotypical variability of expanded alleles in the TATA-binding protein gene
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3. Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17;Cellular and Molecular Life Sciences;2022-04-28
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