{"id":"doi:10.1172/jci92087","kind":"article","title":"CRISPR/Cas9-mediated gene editing ameliorates neurotoxicity in mouse model of Huntington’s disease","authors":["Su Yang","Renbao Chang","Huiming Yang","Ting Zhao","Yan Hong","Ha Eun Kong","Xiaobo Sun","Zhaohui Steve Qin","Peng Jin","Shihua Li","Xiao‐Jiang Li"],"author_count":11,"year":2017,"published":"2017-06-18","venue":"Journal of Clinical Investigation","cited_by":400,"doi":"10.1172/jci92087","arxiv_id":null,"nct_id":null,"source_url":"https://doi.org/10.1172/jci92087","archive_url":"https://space-kitty.com/papers/doi:10.1172/jci92087","updated":null,"pmid":"28628038","pmcid":null,"openalex_id":"W2626238587","pdf_url":"http://www.jci.org/articles/view/92087/files/pdf","abstract":null,"abstract_license":null,"license":null,"is_open_access":true,"retracted":false,"peer_reviewed":null,"categories":["Genetic Neurodegenerative Diseases"],"details":null,"provenance":"openalex","attribution":"Metadata and citation counts: OpenAlex (CC0).","topics":[{"slug":"gene-editing-therapies","name":"CRISPR & Gene-Editing Therapies","domain_slug":"medicine"}],"cited_in_dossiers":[]}