Article Versions Notes

Gaweda-Walerych K, Sitek EJ, Borczyk M, Narożańska E, Brockhuis B, Korostyński M, Schinwelski M, Siemiński M, Sławek J, Zekanowski C. A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in ATP7B, SETX, SORL1, and FOXP1 Genes. Genes. 2022; 13(12):2361. https://doi.org/10.3390/genes13122361

Gaweda-Walerych, Katarzyna, Emilia J. Sitek, Małgorzata Borczyk, Ewa Narożańska, Bogna Brockhuis, Michał Korostyński, Michał Schinwelski, Mariusz Siemiński, Jarosław Sławek, and Cezary Zekanowski. 2022. "A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in ATP7B, SETX, SORL1, and FOXP1 Genes" Genes 13, no. 12: 2361. https://doi.org/10.3390/genes13122361

Gaweda-Walerych, K., Sitek, E. J., Borczyk, M., Narożańska, E., Brockhuis, B., Korostyński, M., Schinwelski, M., Siemiński, M., Sławek, J., & Zekanowski, C. (2022). A Patient with Corticobasal Syndrome and Progressive Non-Fluent Aphasia (CBS-PNFA), with Variants in ATP7B, SETX, SORL1, and FOXP1 Genes. Genes, 13(12), 2361. https://doi.org/10.3390/genes13122361