Europe PMC
open access
Novel CTNNB1 Gene Variants in Spanish CTNNB1 Syndrome Patients: Clinical and Psychological Manifestations
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
- Genotype-phenotype Correlations in Children and Adults With CTNNB1 Mutation#1007327
- CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology#291683
- Role of Genetic Polymorphism in Neuroplasticity Involved in Dysphagia Recovery#1173759
- Mechanisms of genetic variation underlying neurodevelopmental disorder phenotypes in the human cortex#651665
- Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases#844347
Record · ID 651750
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