NCBI PubMed Central
open access
Identification of biallelic loss-of-function PREP variants in three individuals with syndromic intellectual disability.
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
- Pragmatic Impairments#91943
- The Relations Between Recognition Disorders of Familiar People and Other Unique Entities in Patients with Semantic and Behavioral Variants of Right Frontotemporal Degeneration: A Review of Single-Case Studies.#412379
- Executive Function Predicts Self-Injurious Behaviour in Autistic Children With Co-Occurring Intellectual Disability, 2022-2023#419426
- Ultra-rare variants in LAMA2 are risk factors for frontotemporal dementia and motor neuron disease.#218781
- Loss-of-function variants in MARK2 cause neurodevelopmental disorder.#145994
Record · ID 645235
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