Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis | Translational Psychiatry
Simons SearchlightIQSEC2 - Simons Searchlight
Precision medicine for the rescue of specific impairments in social behavior associated with the A350V Iqsec2 mutation | bioRxiv
A Diagnostic Odyssey - Mass General Giving
PDF) IQSEC2 Deficiency Results in Abnormal Social Behaviors Relevant to Autism by Affecting Functions of Neural Circuits in the Medial Prefrontal Cortex
Deep phenotyping of 14 new patients with IQSEC2 variants, including monozygotic twins of discordant phenotype - Radley - 2019 - Clinical Genetics - Wiley Online Library
IJMS | Free Full-Text | IQSEC2-Associated Intellectual Disability and Autism
Structural and Functional Brain-wide Alterations in A350V IQSEC2 Mutant Mice Displaying Autistic-like Behavior | bioRxiv
Fighting Rare Iqsec2 & VWMD Axel & Aria
IQSEC2 Virtual Strollathon
Si raccolgono fondi per un camp inclusivo per bambini disabili e normodotati
tigercece – Associazione AMA.le IQSEC2
IQSEC2 - Research and Advocacy Foundation
IQSEC2 - Research and Advocacy 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
Frontiers | IQSEC2-related encephalopathy in male children: Novel mutations and phenotypes
Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females | Life Science Alliance
Informazione indipendente sulle nuove biotecnologie applicate in ambito medico - Osservatorio Terapie Avanzate - Pagina 134.33333333333
IQSEC2-
AMA.LE PER LA DISABILITÀ | Reale Foundation
IQSEC2 - Research and Advocacy Foundation
Children with intellectual disability – Channel 7 Children's Research Foundation
