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Gabaldón-Albero A, Smeyers P, Hernández-Muela S, Roselló M, Orellana C, Monfort S, Oltra S, Martínez F. Triplication of the PCDH19 Gene as a Novel Disease Mechanism Leading to Epileptic Encephalopathy Resembling Loss-of-Function Pathogenic Variants. Genes. 2024; 15(10):1312. https://doi.org/10.3390/genes15101312

Gabaldón-Albero, Alba, Patricia Smeyers, Sara Hernández-Muela, Mónica Roselló, Carmen Orellana, Sandra Monfort, Silvestre Oltra, and Francisco Martínez. 2024. "Triplication of the PCDH19 Gene as a Novel Disease Mechanism Leading to Epileptic Encephalopathy Resembling Loss-of-Function Pathogenic Variants" Genes 15, no. 10: 1312. https://doi.org/10.3390/genes15101312

Gabaldón-Albero, A., Smeyers, P., Hernández-Muela, S., Roselló, M., Orellana, C., Monfort, S., Oltra, S., & Martínez, F. (2024). Triplication of the PCDH19 Gene as a Novel Disease Mechanism Leading to Epileptic Encephalopathy Resembling Loss-of-Function Pathogenic Variants. Genes, 15(10), 1312. https://doi.org/10.3390/genes15101312