Correction : Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia

enthalten in: European journal of human genetics : EJHG | 2023

von Kesim, Y. | Ceroni, F. | Damián, A. | +12

Correction : VIsoQLR: an interactive tool for the detection, quantification and fine-tuning of isoforms in selected genes using long-read sequencing

enthalten in: Human genetics | 2023

von Núñez-Moreno, G. | Tamayo, A. | Ruiz-Sánchez, C. | +2

Author Correction : Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

enthalten in: Scientific reports | 2021

von Perea-Romero, I. | Gordo, G. | Iancu, I. | +114

Correction : Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2019

von Van de Sompele, S. | Smith, C. | Karali, M. | +24

Corrigendum : Panel-based NGS Reveals Novel Pathogenic Mutations in Autosomal Recessive Retinitis Pigmentosa

enthalten in: Scientific reports | 2016

von Perez-Carro, R. | Corton, M. | Sánchez-Navarro, I. | +14

Correction : Exome Sequencing of Index Patients with Retinal Dystrophies as a Tool for Molecular Diagnosis

enthalten in: PloS one | 2016

von Corton, M. | Nishiguchi, K. | Avila-Fernández, A. | +5