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Bukvic N, De Rinaldis M, Chetta M, Trabacca A, Bassi MT, Marsano RM, Holoubkova L, Rivieccio M, Oro M, Resta N, et al. De Novo Pathogenic Variant in FBRSL1, Non OMIM Gene Paralogue AUTS2, Causes a Novel Recognizable Syndromic Manifestation with Intellectual Disability; An Additional Patient and Review of the Literature. Genes. 2024; 15(7):826. https://doi.org/10.3390/genes15070826

Bukvic, Nenad, Marta De Rinaldis, Massimiliano Chetta, Antonio Trabacca, Maria Teresa Bassi, René Massimiliano Marsano, Lenka Holoubkova, Maria Rivieccio, Maria Oro, Nicoletta Resta, and et al. 2024. "De Novo Pathogenic Variant in FBRSL1, Non OMIM Gene Paralogue AUTS2, Causes a Novel Recognizable Syndromic Manifestation with Intellectual Disability; An Additional Patient and Review of the Literature" Genes 15, no. 7: 826. https://doi.org/10.3390/genes15070826

Bukvic, N., De Rinaldis, M., Chetta, M., Trabacca, A., Bassi, M. T., Marsano, R. M., Holoubkova, L., Rivieccio, M., Oro, M., Resta, N., Kerkhof, J., Sadikovic, B., & Viggiano, L. (2024). De Novo Pathogenic Variant in FBRSL1, Non OMIM Gene Paralogue AUTS2, Causes a Novel Recognizable Syndromic Manifestation with Intellectual Disability; An Additional Patient and Review of the Literature. Genes, 15(7), 826. https://doi.org/10.3390/genes15070826