Article Versions Notes

Larasati YA, Solis GP, Koval A, Griffiths ST, Berentsen R, Aukrust I, Lesca G, Chatron N, Ville D, Korff CM, et al. Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing GNAO1 Mutation P170R. Cells. 2023; 12(20):2469. https://doi.org/10.3390/cells12202469

Larasati, Yonika A., Gonzalo P. Solis, Alexey Koval, Silja T. Griffiths, Ragnhild Berentsen, Ingvild Aukrust, Gaetan Lesca, Nicolas Chatron, Dorothée Ville, Christian M. Korff, and et al. 2023. "Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing GNAO1 Mutation P170R" Cells 12, no. 20: 2469. https://doi.org/10.3390/cells12202469

Larasati, Y. A., Solis, G. P., Koval, A., Griffiths, S. T., Berentsen, R., Aukrust, I., Lesca, G., Chatron, N., Ville, D., Korff, C. M., & Katanaev, V. L. (2023). Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing GNAO1 Mutation P170R. Cells, 12(20), 2469. https://doi.org/10.3390/cells12202469