NCBI PubMed Central
open access
Structural characterization of the human CC2D1A fragment associated with non-syndromic intellectual disability (NSID).
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Variants in DENND2B are associated with vulnerability for neurodevelopmental impairment, psychosis and catatonia#304449
- The Sherpa hypothesis: Phenotype-Preserving Disordered Proteins stabilize the phenotypes of neurons and oligodendrocytes#1066104
- Phase II Clinical Trial to Evaluate the Efficacy and Safety of NV01-A02 in Children With Autism Spectrum Disorder#843751
- Autism-associated NRXN1α deletion rewires the H3K27me3 landscape and epigenetically disrupts human neural induction.#633092
- Identification and Validation of the Nrf2/Slc2a1 Axis in Alzheimer's Disease#1133212
Record · ID 227702
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive