Referenced in: none

Automatically associated channels: SK2

Title: Uncovering a Role for SK2 in Angelman Syndrome.

Authors: Sofia B Lizarraga, Eric M Morrow

Journal, date & volume: Cell Rep, 2015 Jul 21 , 12, 359-60

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26200312

Abstract
Angelman syndrome is a severe neurodevelopmental disorder caused by mutations in UBE3A. Sun et al. (2015) report SK2 as a UBE3A substrate and provide insight into the molecular mechanisms that might underlie impaired neuronal function in individuals affected by Angelman syndrome.