Erratum to “Identification of Novel Nonsense RPGR Variant Causing Mild X-Linked Cone-Rod Dystrophy and Myopia” [Case Reports in Clinical Medicine Volume 11 (2022) 422-434]

Kunka Kamenarova^1,2, Sylvia Cherninkova³, Kalina Mihova^1,2, Rosen Georgiev⁴, Yana Nikolaeva⁵, Radka Kaneva^1,2

¹Molecular Medicine Center, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University—Sofia, Sofia, Bulgaria.
²Laboratory of Genomic Diagnostics, Department of Medical Chemistry and Biochemistry, Medical Faculty, Medical University—Sofia, Sofia, Bulgaria.
³Clinic of Nervous diseases, University Hospital “Alexandrovska”, Sofia, Bulgaria.
⁴Clinic of Eye Diseases, University Hospital “Alexandrovska”, Sofia, Bulgaria.
⁵Eye Clinic “Vision”, Sofia, Bulgaria.

DOI: 10.4236/crcm.2024.133009                

Abstract

The original online version of this article (Kamenarova, K., Cherninkova, S., Mihova, K., Georgiev, R., Nikolaeva, Y. and Kaneva, R. (2022) Identification of Novel Nonsense RPGR Variant Causing Mild X-Linked Cone-Rod Dystrophy and Myopia. Case Reports in Clinical Medicine, 11, 422-434. DOI: 10.4236/crcm.2022.1110059) unfortunately contains a mistake. The authors need to replace Figure 1.

Keywords

Erratum

Figure 1. Pedigree of CRD family and segregation analysis of identified mutation c.1905 + 223C > T in RPGRORF15. Individuals are identified by pedigree number. Squares indicate males, circles indicate females, slashed symbols indicate deceased, solid symbols indicate affected individuals, open symbols indicate unaffected individuals, black arrow indicates the proband. Sequencing chromatograms showing mutation segregation in the pedigree are presented.

Conflicts of Interest

The authors declare no conflicts of interest.

References