The SATB2 Gene Foundation prioritizes the following areas in SAS research, based on high impact needs identified by a recent independent scientific analysis and caregiver input:
- Speech and Language
- Behavior
- Sleep
- Global Development Delays
Additional research priorities include projects on SATB2 function and expression, variations in clinical phenotypes, and symptomatic and/or curative therapeutic interventions. We support projects that gather foundational knowledge about SATB2 function, and we also support projects that aim for tangible and immediate clinical applicability.
In addition, the SATB2 Gene Foundation has previously supported other research resources, such as iPSCs for a variety of precise SATB2 mutations. Please reach out if access to these resources may be helpful to your research.