Dual-isoform hUBE3A gene transfer improves behavioral and seizure outcomes in Angelman syndrome model mice
Author:
Funder
Angelman Syndrome Foundation
NICHD
NIMH
NINDS
NIH
NIH-NINDS
NIH_NICHD
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://insight.jci.org/articles/view/144712/files/pdf
Reference87 articles.
1. Angelman syndrome — insights into a rare neurogenetic disorder
2. Seizure treatment in Angelman syndrome: A case series from the Angelman Syndrome Clinic at Massachusetts General Hospital
3. From UBE3A to Angelman syndrome: a substrate perspective;Sell;Front Neurosci,2015
4. Angelman syndrome–associated point mutations in the Zn2+-binding N-terminal (AZUL) domain of UBE3A ubiquitin ligase inhibit binding to the proteasome
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