Title : Cloning and expression analysis of the murine homolog of the spinocerebellar ataxia type 7 (SCA7) gene.

Pub. Date : 2002 Feb 20

PMID : 12039035






3 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disease caused by the expansion of a polyglutamine tract in the protein ataxin-7, a protein of unknown function. polyglutamine ataxin 7 Mus musculus
2 Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disease caused by the expansion of a polyglutamine tract in the protein ataxin-7, a protein of unknown function. polyglutamine ataxin 7 Mus musculus
3 Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disease caused by the expansion of a polyglutamine tract in the protein ataxin-7, a protein of unknown function. polyglutamine ataxin 7 Mus musculus