Gabaldón-Albero, A.; Smeyers, P.; Hernández-Muela, S.; Roselló, M.; Orellana, C.; Monfort, S.; Oltra, S.; MartÃnez, F.
Triplication of the PCDH19 Gene as a Novel Disease Mechanism Leading to Epileptic Encephalopathy Resembling Loss-of-Function Pathogenic Variants. Genes 2024, 15, 1312.
https://doi.org/10.3390/genes15101312
AMA Style
Gabaldón-Albero A, Smeyers P, Hernández-Muela S, Roselló M, Orellana C, Monfort S, Oltra S, MartÃnez 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
Chicago/Turabian Style
Gabaldón-Albero, Alba, Patricia Smeyers, Sara Hernández-Muela, Mónica Roselló, Carmen Orellana, Sandra Monfort, Silvestre Oltra, and Francisco MartÃnez.
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
APA Style
Gabaldón-Albero, A., Smeyers, P., Hernández-Muela, S., Roselló, M., Orellana, C., Monfort, S., Oltra, S., & MartÃnez, 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
