Ophthalmic Genetics
Volume 43, 2022 - Issue 3
Research Report
Novel RCBTB1 variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophy
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Brian G. Balliosb Ocular Genomics Institute, Department of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA;c Department of Ophthalmology and Vision Sciences, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canadahttps://orcid.org/0000-0002-4644-3339View further author information
https://orcid.org/0000-0002-4644-3339View further author information, , Naomi E. Wagnerb Ocular Genomics Institute, Department of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USAhttps://orcid.org/0000-0002-5470-2652View further author information
https://orcid.org/0000-0002-5470-2652View further author information, , Eric A. Pierceb Ocular Genomics Institute, Department of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USAhttps://orcid.org/0000-0002-2354-4102View further author information
https://orcid.org/0000-0002-2354-4102View further author information, , & Rachel M. Huckfeldtb Ocular Genomics Institute, Department of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USACorrespondence[email protected]
https://orcid.org/0000-0002-9220-2261View further author information
https://orcid.org/0000-0002-9220-2261View further author information show all