Teralı, K. Et Al. 2024. Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome. CTS-CLINICAL AND TRANSLATIONAL SCIENCE , vol.17, no.1 .

Teralı, K., Türkyılmaz, A., Sağer, S. G., & Çebi, A. H., (2024). Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome. CTS-CLINICAL AND TRANSLATIONAL SCIENCE , vol.17, no.1.

Teralı, Kerem Et Al. "Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome," CTS-CLINICAL AND TRANSLATIONAL SCIENCE , vol.17, no.1, 2024

Teralı, Kerem Et Al. "Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome." CTS-CLINICAL AND TRANSLATIONAL SCIENCE , vol.17, no.1, 2024

Teralı, K. Et Al. (2024) . "Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome." CTS-CLINICAL AND TRANSLATIONAL SCIENCE , vol.17, no.1.

@article{article, author={Kerem Teralı Et Al. }, title={Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome}, journal={CTS-CLINICAL AND TRANSLATIONAL SCIENCE}, year=2024}