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CRISPR/Cas9 gene editing reverses Huntington's in mouse model

12:00 EDT 19 Jun 2017 | Medical Xpress

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, scientists report.

Original Article: CRISPR/Cas9 gene editing reverses Huntington's in mouse model

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