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

Affiliations

• ¹ Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.
• ² Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
• ³ Department of Genetics & Genomics, Instituto de Investigación Sanitaria-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), Madrid, Spain.
• ⁴ Centre for Biomedical Network Research on Rare Diseases (CIBERER), Madrid, Spain.
• ⁵ MRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Edinburgh, UK.
• ⁶ Department of Medical Genetics, Nice Teaching Hospital, Nice, France.
• ⁷ INSERM U1214, ToNIC, Université Toulouse III, Toulouse, France.
• ⁸ Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, CHU Toulouse, Toulouse, France.
• ⁹ Department of Human Genetics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
• ¹⁰ Department of Pediatrics, RAZI-CLINIC Hospital, Tangier, Morocco.
• ¹¹ Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK. nragge@brookes.ac.uk.
• ¹² Department of Clinical Genetics, West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women's and Children's Foundation Trust, Birmingham, UK. nragge@brookes.ac.uk.