Error in Classification of Variants

No authors listed

Published Erratum

No authors listed. JAMA Ophthalmol. 2021.

. 2021 Dec 1;139(12):1324.

doi: 10.1001/jamaophthalmol.2021.4737.

No abstract available

Erratum for

Retinal Phenotype of Patients With Isolated Retinal Degeneration Due to CLN3 Pathogenic Variants in a French Retinitis Pigmentosa Cohort.
Smirnov VM, Nassisi M, Solis Hernandez C, Méjécase C, El Shamieh S, Condroyer C, Antonio A, Meunier I, Andrieu C, Defoort-Dhellemmes S, Mohand-Said S, Sahel JA, Audo I, Zeitz C. Smirnov VM, et al. JAMA Ophthalmol. 2021 Mar 1;139(3):278-291. doi: 10.1001/jamaophthalmol.2020.6089. JAMA Ophthalmol. 2021. PMID: 33507216 Free PMC article.
Challenges of Phenotype-Genotype Correlations in Rare Diseases-Reply.
Smirnov VM, Zeitz C, Audo I. Smirnov VM, et al. JAMA Ophthalmol. 2021 Dec 1;139(12):1323-1324. doi: 10.1001/jamaophthalmol.2021.4375. JAMA Ophthalmol. 2021. PMID: 34709364 No abstract available.

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 - PubMed
1. 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