Pub. Date : 2014 Dec 5
PMID : 25316320
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Huntington"s disease (HD) is an autosomal dominant neurodegenerative disorder caused by a mutation in the Huntingtin gene, where excessive (>= 36) CAG repeats encode for glutamine expansion in the huntingtin protein. | Glutamine | huntingtin | Homo sapiens |
2 | Huntington"s disease (HD) is an autosomal dominant neurodegenerative disorder caused by a mutation in the Huntingtin gene, where excessive (>= 36) CAG repeats encode for glutamine expansion in the huntingtin protein. | Glutamine | huntingtin | Homo sapiens |