Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females | Life Science Alliance
tigercece – Associazione AMA.le IQSEC2
Children with intellectual disability – Channel 7 Children's Research Foundation
AMA.LE PER LA DISABILITÀ | Reale Foundation
Ca2+-induced release of IQSEC2/BRAG1 autoinhibition under physiological and pathological conditions | Journal of Cell Biology | Rockefeller University Press
IJMS | Free Full-Text | Molecular Insights into IQSEC2 Disease
IQSEC2 Virtual Strollathon
Deep phenotyping of 14 new patients with IQSEC2 variants, including monozygotic twins of discordant phenotype - Radley - 2019 - Clinical Genetics - Wiley Online Library
IQSEC2 - Research and Advocacy Foundation
Si raccolgono fondi per un camp inclusivo per bambini disabili e normodotati
IJMS | Free Full-Text | IQSEC2-Associated Intellectual Disability and Autism
Simons SearchlightIQSEC2 - Simons Searchlight
Alba ama AMA.le: missione compiuta! – Associazione AMA.le IQSEC2
Kasr Al Ainy Faculty of Medicine International Affairs | Cairo
Frontiers | IQSEC2-related encephalopathy in male children: Novel mutations and phenotypes
AMA.LE PER LA DISABILITÀ | Reale Foundation
IQSEC2-
IQSEC2 - Research and Advocacy Foundation
IQSEC2 - Research and Advocacy Foundation
IQSEC2-
A Diagnostic Odyssey - Mass General Giving
IQSEC2 - Research and Advocacy Foundation
RCSB PDB - 6FAE: The Sec7 domain of IQSEC2 (Brag1) in complex with the small GTPase Arf1
IQSEC2 - Research and Advocacy Foundation
