Title : Degron capability of the hydrophobic C-terminus of the polyglutamine disease protein, ataxin-3.

Pub. Date : 2020 Oct

PMID : 32643791






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Mutations in ataxin-3 cause spinocerebellar ataxia type 3 (SCA3), a neurodegenerative disorder that is a member of the polyglutamine family of diseases. polyglutamine ataxin 3 Homo sapiens
2 Mutations in ataxin-3 cause spinocerebellar ataxia type 3 (SCA3), a neurodegenerative disorder that is a member of the polyglutamine family of diseases. polyglutamine ataxin 3 Homo sapiens