Title : SUPT4H1-edited stem cell therapy rescues neuronal dysfunction in a mouse model for Huntington's disease.

Pub. Date : 2022 Jan 19

PMID : 35046408






3 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Huntington"s disease (HD) is a severe inherited neurological disorder caused by a CAG repeat expansion in the huntingtin gene (HTT), leading to the accumulation of mutant huntingtin with polyglutamine repeats. polyglutamine huntingtin Homo sapiens
2 Huntington"s disease (HD) is a severe inherited neurological disorder caused by a CAG repeat expansion in the huntingtin gene (HTT), leading to the accumulation of mutant huntingtin with polyglutamine repeats. polyglutamine huntingtin Homo sapiens
3 Huntington"s disease (HD) is a severe inherited neurological disorder caused by a CAG repeat expansion in the huntingtin gene (HTT), leading to the accumulation of mutant huntingtin with polyglutamine repeats. polyglutamine huntingtin Homo sapiens