Title : Clinical Features of Huntington's Disease.

Pub. Date : 2018

PMID : 29427096






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The causative genetic mutation is an expanded CAG trinucleotide repeat in the gene encoding the Huntingtin protein, which leads to a prolonged polyglutamine stretch at the N-terminus of the protein. trinucleotide huntingtin Homo sapiens