Pub. Date : 2006 Mar 1
PMID : 16434483
4 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | Huntington"s disease (HD) and spinocerebellar ataxia type 7 (SCA7) belong to a group of inherited neurodegenerative diseases caused by polyglutamine (polyQ) expansion in corresponding proteins. | polyglutamine | ataxin 7 | Mus musculus |
| 2 | Huntington"s disease (HD) and spinocerebellar ataxia type 7 (SCA7) belong to a group of inherited neurodegenerative diseases caused by polyglutamine (polyQ) expansion in corresponding proteins. | polyglutamine | ataxin 7 | Mus musculus |
| 3 | Huntington"s disease (HD) and spinocerebellar ataxia type 7 (SCA7) belong to a group of inherited neurodegenerative diseases caused by polyglutamine (polyQ) expansion in corresponding proteins. | polyglutamine | ataxin 7 | Mus musculus |
| 4 | Huntington"s disease (HD) and spinocerebellar ataxia type 7 (SCA7) belong to a group of inherited neurodegenerative diseases caused by polyglutamine (polyQ) expansion in corresponding proteins. | polyglutamine | ataxin 7 | Mus musculus |