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CRISPR/Cas9 gene editing reverses Huntington's in mouse model
Disrupting a problematic gene in brain cells can reverse Huntington's disease pathology and motor symptoms in a mouse model of the inherited neurological disorder
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| Categories: | Tags: Genetics, genome modification, genetic engineering, synthetic biology, CRISPR, CRISPR/Cas9, Huntington's disease | Comments: (0) | View Count: (985)