NCBI PubMed Central
open access
Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy.
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.
Checking your browser - reCAPTCHA Checking your browser before accessing pmc.ncbi.nlm.nih.gov ... Click here if you are not automatically redirected after 5 seconds.
Related documents
- Neurophysiological Studies in Schizophrenia and Psychiatric Disorders#854052
- Recurrent patterns of TOP1-mediated neuronal genomic damage shared by major neurodegenerative disorders.#351564
- Myelin dysfunction in autism spectrum disorder: insights into core symptoms and mechanisms of brain development#311525
- Preserved Limbic White Matter Predicts Favorable 2‐Year Outcomes in Neonatal Hypoxic‐Ischemic Encephalopathy.#430844
- Targeting type 2 inflammation in dermatology: mechanisms and clinical implications.#630958
Record · ID 25523 · SHA-256 07f195b063891691
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