# Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype

**Authors:** Mingkai Yang, Yanfang Xiao, Chanjuan Chen, Zhou Chu, Guohong Hu

PMC · DOI: 10.3389/fgene.2025.1769021 · Frontiers in Genetics · 2026-01-09

## Full-text entities

- **Genes:** BP2 [NCBI Gene 474257], BP1 [NCBI Gene 474256], ASXL3 (ASXL transcriptional regulator 3) [NCBI Gene 80816] {aka BRPS, KIAA1713}

## Full text

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Source: https://tomesphere.com/paper/PMC12826597