# Corrigendum: Case report and literature review: delayed diagnosis of ARCL1B due to a newly reported homozygous mutation c.464A>C p. (Tyr155Ser) in the EFEMP2 gene

**Authors:** Lixue Ouyang, Fan Yang, Hongyu Duan, Chuan Wang

PMC · DOI: 10.3389/fgene.2025.1589037 · Frontiers in Genetics · 2025-03-13

## Full-text entities

- **Genes:** EFEMP2 (EGF-like fibulin extracellular matrix protein 2) [NCBI Gene 30008] {aka ARCL1B, FBLN4, MBP1, UPH1}
- **Mutations:** c.464A>C, Tyr155Ser

## Full text

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Source: https://tomesphere.com/paper/PMC11947943