Kalampokini, S.; Goulis, D.G.; Pepe, G.; Koukoula, S.; Frontistis, A.; Moschou, M.; Arnaoutoglou, M.; Papaliagkas, V.; Kimiskidis, V.K.
Rare Case with Pathogenic Variant in DHX16 Gene Causing Neuromuscular Disease and Oculomotor Anomalies. Int. J. Mol. Sci. 2025, 26, 2812.
https://doi.org/10.3390/ijms26062812
AMA Style
Kalampokini S, Goulis DG, Pepe G, Koukoula S, Frontistis A, Moschou M, Arnaoutoglou M, Papaliagkas V, Kimiskidis VK.
Rare Case with Pathogenic Variant in DHX16 Gene Causing Neuromuscular Disease and Oculomotor Anomalies. International Journal of Molecular Sciences. 2025; 26(6):2812.
https://doi.org/10.3390/ijms26062812
Chicago/Turabian Style
Kalampokini, Stefania, Dimitrios G. Goulis, Georgia Pepe, Stavrenia Koukoula, Antonis Frontistis, Maria Moschou, Marianthi Arnaoutoglou, Vasileios Papaliagkas, and Vasilios K. Kimiskidis.
2025. "Rare Case with Pathogenic Variant in DHX16 Gene Causing Neuromuscular Disease and Oculomotor Anomalies" International Journal of Molecular Sciences 26, no. 6: 2812.
https://doi.org/10.3390/ijms26062812
APA Style
Kalampokini, S., Goulis, D. G., Pepe, G., Koukoula, S., Frontistis, A., Moschou, M., Arnaoutoglou, M., Papaliagkas, V., & Kimiskidis, V. K.
(2025). Rare Case with Pathogenic Variant in DHX16 Gene Causing Neuromuscular Disease and Oculomotor Anomalies. International Journal of Molecular Sciences, 26(6), 2812.
https://doi.org/10.3390/ijms26062812