Title : Personalized gene silencing therapeutics for Huntington disease.

Pub. Date : 2014 Jul

PMID : 24646433






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Huntington disease (HD) is an autosomal dominant disorder caused by an expanded CAG trinucleotide repeat in the Huntingtin gene (HTT). trinucleotide huntingtin Homo sapiens
2 Huntington disease (HD) is an autosomal dominant disorder caused by an expanded CAG trinucleotide repeat in the Huntingtin gene (HTT). trinucleotide huntingtin Homo sapiens