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Cabrita Pinto RL, Viaggi S, Canale E, Martinez Popple M, Capra V, Conteduca G, Testa B, Coviello D, Covone AE. Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome. Genes. 2023; 14(4):810. https://doi.org/10.3390/genes14040810

Cabrita Pinto, Rute Luísa, Silvia Viaggi, Edoardo Canale, Marina Martinez Popple, Valeria Capra, Giuseppina Conteduca, Barbara Testa, Domenico Coviello, and Angela Elvira Covone. 2023. "Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome" Genes 14, no. 4: 810. https://doi.org/10.3390/genes14040810

Cabrita Pinto, R. L., Viaggi, S., Canale, E., Martinez Popple, M., Capra, V., Conteduca, G., Testa, B., Coviello, D., & Covone, A. E. (2023). Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome. Genes, 14(4), 810. https://doi.org/10.3390/genes14040810