Title : Inhibiting cellular uptake of mutant huntingtin using a monoclonal antibody: Implications for the treatment of Huntington's disease.

Pub. Date : 2020 Jul

PMID : 32407769






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Huntington"s disease (HD) is caused by a highly polymorphic CAG trinucleotide expansion in the gene encoding for the huntingtin protein (HTT). trinucleotide huntingtin Homo sapiens
2 Huntington"s disease (HD) is caused by a highly polymorphic CAG trinucleotide expansion in the gene encoding for the huntingtin protein (HTT). trinucleotide huntingtin Homo sapiens