In the Original Investigation titled “Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to CLN3 Pathogenic Variants in a French Retinitis Pigmentosa Cohort,”1 published online January 28, 2021, and in the March 2021 issue of JAMA Ophthalmology, 2 variants were erroneously classified in the severe neuronal ceroid lipofuscinosis (NCL) group instead of the classic CLN3-associated NCL. The Discussion section and Figure 3 were updated. None of the study’s conclusions were affected. The article was corrected online.2
References
- 1.Smirnov VM, Nassisi M, Solis Hernandez C, et al. Retinal phenotype of patients with isolated retinal degeneration due to CLN3 pathogenic variants in a French retinitis pigmentosa cohort. JAMA Ophthalmol. 2021;139(3):278-291. doi: 10.1001/jamaophthalmol.2020.6089 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Smirnov VM, Zeitz C, Audo I. Challenges of phenotype-genotype correlations in rare diseases—reply. JAMA Ophthalmol. Published online October 28, 2021. doi: 10.1001/jamaophthalmol.2021.4375 [DOI] [PubMed] [Google Scholar]