Title : Reduction of mutant ataxin-7 expression restores motor function and prevents cerebellar synaptic reorganization in a conditional mouse model of SCA7.

Pub. Date : 2013 Mar 1

PMID : 23197655






3 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Spinocerebellar ataxia type 7 (SCA7) is a dominantly inherited neurodegenerative disorder caused by a CAG - polyglutamine (polyQ) repeat expansion in the ataxin-7 gene. polyglutamine ataxin 7 Mus musculus
2 Spinocerebellar ataxia type 7 (SCA7) is a dominantly inherited neurodegenerative disorder caused by a CAG - polyglutamine (polyQ) repeat expansion in the ataxin-7 gene. polyglutamine ataxin 7 Mus musculus
3 Spinocerebellar ataxia type 7 (SCA7) is a dominantly inherited neurodegenerative disorder caused by a CAG - polyglutamine (polyQ) repeat expansion in the ataxin-7 gene. polyglutamine ataxin 7 Mus musculus