A Diagnostic Odyssey - Mass General Giving
IQSEC2 - Research and Advocacy Foundation
IQSEC2-
Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females | Life Science Alliance
Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis | Translational Psychiatry
Alba ama AMA.le: missione compiuta! – Associazione AMA.le IQSEC2
Fundraiser for Associazione AMA.le by Danila Borio : IQSEC2: DONA UN SOSTEGNO ALLA RICERCA
IQSEC2 - Research and Advocacy Foundation
PDF) Natural Course of IQSEC2-Related Encephalopathy: An Italian National Structured Survey
Fighting Rare Iqsec2 & VWMD Axel & Aria
Children with intellectual disability – Channel 7 Children's Research Foundation
RCSB PDB - 6FAE: The Sec7 domain of IQSEC2 (Brag1) in complex with the small GTPase Arf1
Frontiers | IQSEC2-related encephalopathy in male children: Novel mutations and phenotypes
IQSEC2 - Research and Advocacy Foundation
Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females | Life Science Alliance
Simons SearchlightIQSEC2 - Simons Searchlight
Si raccolgono fondi per un camp inclusivo per bambini disabili e normodotati
Precision medicine for the rescue of specific impairments in social behavior associated with the A350V Iqsec2 mutation | bioRxiv
Kasr Al Ainy Faculty of Medicine International Affairs | Cairo
RCSB PDB - 6FAE: The Sec7 domain of IQSEC2 (Brag1) in complex with the small GTPase Arf1
IJMS | Free Full-Text | Molecular Insights into IQSEC2 Disease
IQSEC2-
AMA.LE PER LA DISABILITÀ | Reale Foundation
IJMS | Free Full-Text | IQSEC2-Associated Intellectual Disability and Autism
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 Research Grant Program 2023 — Orphan Disease Center
