K. Teralı 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.," 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.. 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.. 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.," 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.." 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.." 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={Clinical and translational science}, year=2024}