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
BMC Med Genomics. 2025 Aug 4;18(1):126.
doi: 10.1186/s12920-025-02197-2.
1 Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
2 Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran.
3 Department of Research and Development, Harmonic Medical Genetics Lab, Isfahan, Iran.
4 Isfahan Eye Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
5 Department of Ophthalmology, Isfahan University of Medical Sciences, Isfahan, Iran.
6 Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran. tabatabaiefar@med.mui.ac.ir.
7 Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran. tabatabaiefar@med.mui.ac.ir.
8 University of Medical Sciences, Isfahan, 81746-73461, Iran. tabatabaiefar@med.mui.ac.ir.