APA (7th ed.) Citation

Maljevic, S., Vejzovic, S., Bernhard, M. K., Bertsche, A., Weise, S., Döcker, M., . . . Syrbe, S. (2016). Novel KCNQ3 muation in a large family with benign familial neonatal epilepsy: A rare cause of neonatal seizures. Molecular syndromology, 7(4), . https://doi.org/10.1159/000447461

Chicago Style (17th ed.) Citation

Maljevic, Snezana, et al. "Novel KCNQ3 Muation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures." Molecular Syndromology 7, no. 4 (2016). https://doi.org/10.1159/000447461.

MLA (9th ed.) Citation

Maljevic, Snezana, et al. "Novel KCNQ3 Muation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures." Molecular Syndromology, vol. 7, no. 4, 2016, https://doi.org/10.1159/000447461.