Human Genome Epidemiology Literature Finder
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Query Trace: Retinal Dystrophies and RCBTB1[original query] |
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Novel RCBTB1 variants causing later-onset non-syndromic retinal dystrophy with macular chorioretinal atrophy. Ophthalmic genetics 2022 1 43 (3): 332-339. Catomeris Andrew J, Ballios Brian G, Sangermano Riccardo, Wagner Naomi E, Comander Jason I, Pierce Eric A, Place Emily M, Bujakowska Kinga M, Huckfeldt Rachel |
- Page last reviewed:Feb 1, 2024
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