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Literature - Publication Review
Utility of engineered human Neural Stem Cells (NSCs) expressing varying exon 1 HTT fragments to study Huntington’s disease
Huntington's disease is most commonly caused by an expansion mutation in the CAG trinucleotide repeat within exon 1 of the HTT gene which codes for the protein huntingtin.
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In vivo imaging solutions
Comprehensive preclinical in vivo imaging solutions from Revvity, featuring instruments, reagents, and application support to advance your research and development studies.
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