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Baz-Red\'f3n N, S\'e1nchez-Bellver L, Fern\'e1ndez-Cancio M, et al. Primary Ciliary Dyskinesia and Retinitis Pigmentosa: Novel  Variant and Possible Modifier Gene. Cells. 2024;13(6). doi:10.3390/cells13060524.\par \par Corton M, Avila-Fern\'e1ndez A, Campello L, et al. Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa. Sci Rep. 2016;6:35370. doi:10.1038/srep35370.\par \par Bravo-Gil N, M\'e9ndez-Vidal C, Romero-P\'e9rez L, et al. Improving the management of Inherited Retinal Dystrophies by targeted sequencing of a population-specific gene panel. Sci Rep. 2016;6:23910. doi:10.1038/srep23910.\par \par M\'e9ndez-Vidal C, Bravo-Gil N, del Pozo MGonz\'e1lez-, et al. Novel RP1 mutations and a recurrent BBS1 variant explain the co-existence of two distinct retinal phenotypes in the same pedigree. BMC Genet. 2014;15:143. doi:10.1186/s12863-014-0143-2.\par \par Barrag\'e1n I, Borrego S, Pieras JIgnacio, et al. Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa. Hum Mutat. 2010;31(11):E1772-800. doi:10.1002/humu.21334.\par \par }