Title : An ovine transgenic Huntington's disease model.

Pub. Date : 2010 May 15

PMID : 20154343






4 Functional Relationships(s)
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Protein Name
Organism
1 Huntington"s disease (HD) is an inherited autosomal dominant neurodegenerative disorder caused by an expansion of a CAG trinucleotide repeat in the huntingtin (HTT) gene [Huntington"s Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington"s disease chromosomes. trinucleotide huntingtin Homo sapiens
2 Huntington"s disease (HD) is an inherited autosomal dominant neurodegenerative disorder caused by an expansion of a CAG trinucleotide repeat in the huntingtin (HTT) gene [Huntington"s Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington"s disease chromosomes. trinucleotide huntingtin Homo sapiens
3 Huntington"s disease (HD) is an inherited autosomal dominant neurodegenerative disorder caused by an expansion of a CAG trinucleotide repeat in the huntingtin (HTT) gene [Huntington"s Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington"s disease chromosomes. trinucleotide huntingtin Homo sapiens
4 Huntington"s disease (HD) is an inherited autosomal dominant neurodegenerative disorder caused by an expansion of a CAG trinucleotide repeat in the huntingtin (HTT) gene [Huntington"s Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington"s disease chromosomes. trinucleotide huntingtin Homo sapiens