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filingDate 2015-08-04^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ec803e971e887b4509e07f0b6a5e801
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publicationDate 2016-02-11^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2993459-A1
titleOfInvention Genome editing for the treatment of huntington's disease
abstract The invention relates to the treatment of Huntington's disease (HD) using the Clustered- Regularly Interspaced Short Palindromic Repeats (CRISPR) system. This technology offers the possibility to design a small RNA (sg RNA), which is incorporated into a CRISPR- associated protein (Cas9) to recognize and induce DNA double-strand breaks at a specific target location. In the context of HD, this allows to block the expression of the mutant huntingtin or repair the CAG expansion causing the disease.
priorityDate 2014-08-04^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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