Pub. Date : 2008 Apr
PMID : 17971076
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Spinocerebellar ataxia type 7 (SCA7) represents a rare and severe autosomal dominantly inherited ataxic disorder and is among the known CAG-repeat, or polyglutamine, diseases. | polyglutamine | ataxin 7 | Homo sapiens |
2 | Spinocerebellar ataxia type 7 (SCA7) represents a rare and severe autosomal dominantly inherited ataxic disorder and is among the known CAG-repeat, or polyglutamine, diseases. | polyglutamine | ataxin 7 | Homo sapiens |