Evolving CRISPR-Cas9 techniques can now be used to edit the HD gene in a living mouse brain.
HDBuzz summarises all the science from the 2017 Huntington's Disease Therapeutics Conference in Malta - day 2
Work with genome editing techniques (zinc fingers and CRISPR) brings these tools closer to use in HD clinical trials
Strategies for getting rid of mutant huntingtin & clinical trial updates: day 2 of the HD therapeutics conference
The news has recently been full of stories about CRISPR, a new "jaw-dropping" DNA-editing technology. Hype or hope?