rAAV-CRISPRa therapy corrects Rai1 haploinsufficiency and rescues selective disease features in Smith-Magenis syndrome mice
Author:
Funder
Simons Foundation
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference53 articles.
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5. Early adolescent Rai1 reactivation reverses transcriptional and social interaction deficits in a mouse model of Smith-Magenis syndrome;Huang;Proc. Natl. Acad. Sci. U. S. A.,2018
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