Title : Amplification of neurotoxic HTTex1 assemblies in human neurons.

Pub. Date : 2021 Nov

PMID : 34563643






4 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Huntington"s disease (HD) is a genetically inherited neurodegenerative disorder caused by expansion of a polyglutamine (polyQ) repeat in the exon-1 of huntingtin protein (HTT). polyglutamine huntingtin Homo sapiens
2 Huntington"s disease (HD) is a genetically inherited neurodegenerative disorder caused by expansion of a polyglutamine (polyQ) repeat in the exon-1 of huntingtin protein (HTT). polyglutamine huntingtin Homo sapiens
3 Huntington"s disease (HD) is a genetically inherited neurodegenerative disorder caused by expansion of a polyglutamine (polyQ) repeat in the exon-1 of huntingtin protein (HTT). polyglutamine huntingtin Homo sapiens
4 Huntington"s disease (HD) is a genetically inherited neurodegenerative disorder caused by expansion of a polyglutamine (polyQ) repeat in the exon-1 of huntingtin protein (HTT). polyglutamine huntingtin Homo sapiens