Maljevic, S., Vejzovic, S., Bernhard, M. K., Bertsche, A., Weise, S., Döcker, M., . . . Syrbe, S. (2016). Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures. Mol Syndromol.
Chicago Style CitationMaljevic, Snezana, et al. "Novel KCNQ3 Mutation in a Large Family With Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures." Mol Syndromol 2016.
Cita MLAMaljevic, Snezana, et al. "Novel KCNQ3 Mutation in a Large Family With Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures." Mol Syndromol 2016.
Atenció: Aquestes cites poden no estar 100% correctes.