Title : Haplotype-based stratification of Huntington's disease.

Pub. Date : 2017 Nov

PMID : 28832564






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Huntington"s disease (HD) is an autosomal dominant neurodegenerative disease caused by expansion of a CAG trinucleotide repeat in HTT, resulting in an extended polyglutamine tract in huntingtin. trinucleotide huntingtin Homo sapiens
2 Huntington"s disease (HD) is an autosomal dominant neurodegenerative disease caused by expansion of a CAG trinucleotide repeat in HTT, resulting in an extended polyglutamine tract in huntingtin. trinucleotide huntingtin Homo sapiens