Title : From Pathogenesis to Novel Therapeutics for Spinocerebellar Ataxia Type 3: Evading Potholes on the Way to Translation.

Pub. Date : 2019 Oct

PMID : 31691128






3 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is a neurodegenerative disorder caused by a polyglutamine expansion in the ATXN3 gene. polyglutamine ataxin 3 Homo sapiens
2 Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is a neurodegenerative disorder caused by a polyglutamine expansion in the ATXN3 gene. polyglutamine ataxin 3 Homo sapiens
3 Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is a neurodegenerative disorder caused by a polyglutamine expansion in the ATXN3 gene. polyglutamine ataxin 3 Homo sapiens