Title : Comparison of spinocerebellar ataxia type 3 mouse models identifies early gain-of-function, cell-autonomous transcriptional changes in oligodendrocytes.

Pub. Date : 2017 Sep 1

PMID : 28854700






3 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene. polyglutamine ataxin 3 Mus musculus
2 Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene. polyglutamine ataxin 3 Mus musculus
3 Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder caused by a polyglutamine-encoding CAG repeat expansion in the ATXN3 gene. polyglutamine ataxin 3 Mus musculus