Pub. Date : 2015 Dec
PMID : 26210848
3 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
| 1 | UNLABELLED: Huntington"s disease (HD) is an autosomal dominant, progressive neurodegenerative disorder, caused by an expanded trinucleotide CAG sequence of the huntingtin (Htt) gene, which encodes a stretch of glutamines in the Htt protein. | Glutamine | huntingtin | Homo sapiens |
| 2 | UNLABELLED: Huntington"s disease (HD) is an autosomal dominant, progressive neurodegenerative disorder, caused by an expanded trinucleotide CAG sequence of the huntingtin (Htt) gene, which encodes a stretch of glutamines in the Htt protein. | Glutamine | huntingtin | Homo sapiens |
| 3 | UNLABELLED: Huntington"s disease (HD) is an autosomal dominant, progressive neurodegenerative disorder, caused by an expanded trinucleotide CAG sequence of the huntingtin (Htt) gene, which encodes a stretch of glutamines in the Htt protein. | Glutamine | huntingtin | Homo sapiens |