| Literature DB >> 35751791 |
Aishika Datta1, Deepaneeta Sarmah1, Harpreet Kaur1, Antra Chaudhary1, Namrata Vadak1, Anupom Borah2, Sudhir Shah3, Xin Wang4, Pallab Bhattacharya5.
Abstract
Neurological disorders have complicated pathophysiology that may involve several genetic mutations. Conventional treatment has limitations as they only treat apparent symptoms. Although, personalized medicine is emerging as a promising neuro-intervention, lack of precision is the major pitfall. Clustered regularly interspaced short palindromic repeat (CRISPR)/Cas9 system is evolving as a technological platform that may overcome the therapeutic limitations towards precision medicine. In the future, targeting genes in neurological disorders may be the mainstay of modern therapy. The present review on CRISPR/Cas9 and its application in various neurological disorders may provide a platform for its future clinical relevance towards developing precise and personalized medicine.Entities:
Keywords: CRISPR/Cas; Genome editing tools; Neurological disorders; TALENs; ZFNs
Year: 2022 PMID: 35751791 DOI: 10.1007/s10571-022-01242-3
Source DB: PubMed Journal: Cell Mol Neurobiol ISSN: 0272-4340 Impact factor: 5.046