Title : Autophagy in Spinocerebellar ataxia type 2, a dysregulated pathway, and a target for therapy.

Pub. Date : 2021 Nov 29

PMID : 34845184






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The mutation causing SCA2 disease is an abnormal expansion of CAG trinucleotide repeats in the ATXN2 gene, leading to a toxic expanded polyglutamine segment in the translated ataxin-2 protein. polyglutamine ataxin 2 Homo sapiens
2 The mutation causing SCA2 disease is an abnormal expansion of CAG trinucleotide repeats in the ATXN2 gene, leading to a toxic expanded polyglutamine segment in the translated ataxin-2 protein. polyglutamine ataxin 2 Homo sapiens