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
Crossref DOI link: https://doi.org/10.1186/s12920-025-02197-2
Published Online: 2025-08-04
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Nouri, Zahra
Sarmadi, Akram
Narrei, Sina
Kianersi, Hamidreza
Kianersi, Farzan
Tabatabaiefar, Mohammad Amin
Text and Data Mining valid from 2025-08-04
Version of Record valid from 2025-08-04
Article History
First Online: 4 August 2025