# Correction: Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia

**Authors:** Zahra Nouri, Akram Sarmadi, Sina Narrei, Hamidreza Kianersi, Farzan Kianersi, Mohammad Amin Tabatabaiefar

PMC · DOI: 10.1186/s12920-025-02197-2 · 2025-08-04

## Full-text entities

- **Genes:** PDE6C (phosphodiesterase 6C) [NCBI Gene 5146] {aka ACHM5, COD4, PDEA2}, PDZD7 (PDZ domain containing 7) [NCBI Gene 79955] {aka DFNB57, PDZK7}
- **Diseases:** non-syndromic hearing loss (MESH:C537845), achromatopsia (MESH:D003117)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12323168/full.md

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Source: https://tomesphere.com/paper/PMC12323168