IQSEC2-
IQSEC2-
Alba ama AMA.le: missione compiuta! – Associazione AMA.le IQSEC2
IQSEC2 - Research and Advocacy Foundation
IQSEC2 Virtual Strollathon
Ca2+-induced release of IQSEC2/BRAG1 autoinhibition under physiological and pathological conditions | Journal of Cell Biology | Rockefeller University Press
IQSEC2 - Research and Advocacy Foundation
RCSB PDB - 6FAE: The Sec7 domain of IQSEC2 (Brag1) in complex with the small GTPase Arf1
Kasr Al Ainy Faculty of Medicine International Affairs | Cairo
IQSEC2 Research and Advocacy Foundation Research Grant Program 2023 — Orphan Disease Center
IJMS | Free Full-Text | Molecular Insights into IQSEC2 Disease
AMA.LE PER LA DISABILITÀ | Reale Foundation
RCSB PDB - 6FAE: The Sec7 domain of IQSEC2 (Brag1) in complex with the small GTPase Arf1
IJMS | Free Full-Text | IQSEC2-Associated Intellectual Disability and Autism
tigercece – Associazione AMA.le IQSEC2
Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females | Life Science Alliance
PDF) Natural Course of IQSEC2-Related Encephalopathy: An Italian National Structured Survey
IQSEC2 - Research and Advocacy Foundation
Si raccolgono fondi per un camp inclusivo per bambini disabili e normodotati
PDF) IQSEC2 Deficiency Results in Abnormal Social Behaviors Relevant to Autism by Affecting Functions of Neural Circuits in the Medial Prefrontal Cortex
Structural and Functional Brain-wide Alterations in A350V IQSEC2 Mutant Mice Displaying Autistic-like Behavior | bioRxiv
AMA.LE PER LA DISABILITÀ | Reale Foundation
Deep phenotyping of 14 new patients with IQSEC2 variants, including monozygotic twins of discordant phenotype - Radley - 2019 - Clinical Genetics - Wiley Online Library
