# Corrigendum: Novel FOXL2 variants in two Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome

**Authors:** Mingyu Zhao, Xiaolu Meng, Jiaqi Wang, Tailing Wang

PMC · DOI: 10.3389/fgene.2024.1414939 · 2024-04-29

## Full-text entities

- **Genes:** FOXL2 (forkhead box L2) [NCBI Gene 668] {aka BPES, BPES1, PFRK, PINTO, POF3}
- **Diseases:** blepharophimosis (MESH:D016569), ptosis (MESH:C564553), epicanthus inversus syndrome (MESH:C562419)

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Source: https://tomesphere.com/paper/PMC11089390