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

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作者单位: Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium. [1] Section of Ophthalmology and Neuroscience, School of Medicine, University of Leeds, St James's University Hospital, Leeds, UK. [2] Medical Genetics, Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy. [3] Telethon Institute of Genetics and Medicine, Pozzuoli, Italy. [4] Genetics Department, Instituto de Investigación Sanitaria-Fundación Jimenez Diaz University Hospital (IIS-FJD, UAM), Madrid, Spain. [5] Center of Biomedical Network Research on Rare Diseases (CIBERER), ISCIII, Madrid, Spain. [6] Department of Medical Protein Research, Faculty of Medicine and Health Sciences, Flanders Institute for Biotechnology (VIB), Ghent University, Ghent, Belgium. [7] Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA, USA. [8] Department of Ophthalmology, St. James's University Hospital, Leeds, UK. [9] Eye Clinic, Multidisciplinary Department of Medical, Surgical and Dental Sciences, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy. [10] Department of Ophthalmology, Fundación Jimenez Diaz University Hospital, Madrid, Spain. [11] Department of Ophthalmology, Ghent University and Ghent University Hospital, Ghent, Belgium. [12] Center for Medical Genetics, Antwerp University Hospital, Antwerp, Belgium. [13] Division of Ophthalmology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA. [14] Medical Genetics, Department of Precision Medicine, Università degli Studi della Campania "Luigi Vanvitelli", Naples, Italy. banfi@tigem.it. [15] Telethon Institute of Genetics and Medicine, Pozzuoli, Italy. banfi@tigem.it. [16] Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium. elfride.debaere@ugent.be. [17]
DOI 10.1038/s41436-018-0392-y
PMID 30607024
发布时间 2022-02-11
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Genetics in medicine : official journal of the American College of Medical Genetics

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