Title : Advances in huntington disease drug discovery: novel approaches to model disease phenotypes.

Pub. Date : 2014 Feb

PMID : 24196395






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Huntington disease is a monogenic, autosomal dominant, progressive neurodegenerative disorder caused by a trinucleotide CAG repeat expansion in exon 1 of the huntingtin (HTT) gene; age of onset of clinical symptoms inversely correlates with expanded CAG repeat length. trinucleotide huntingtin Homo sapiens
2 Huntington disease is a monogenic, autosomal dominant, progressive neurodegenerative disorder caused by a trinucleotide CAG repeat expansion in exon 1 of the huntingtin (HTT) gene; age of onset of clinical symptoms inversely correlates with expanded CAG repeat length. trinucleotide huntingtin Homo sapiens