APA
Soldovieri M. V., Boutry-Kryza N., Milh M., Doummar D., Heron B., Bourel E., Ambrosino P., Miceli F., De Maria M., Dorison N., Auvin S., Echenne B., Oertel J., Riquet A., Lambert L., Gerard M., Roubergue A., Calender A., Mignot C., Taglialatela M. & Lesca G. (20141006). Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A. : Human mutation.
Chicago
Soldovieri Maria Virginia, Boutry-Kryza Nadia, Milh Mathieu, Doummar Diane, Heron Benedicte, Bourel Emilie, Ambrosino Paolo, Miceli Francesco, De Maria Michela, Dorison Nathalie, Auvin Stephane, Echenne Bernard, Oertel Julie, Riquet Audrey, Lambert Laetitia, Gerard Marion, Roubergue Anne, Calender Alain, Mignot Cyril, Taglialatela Maurizio and Lesca Gaetan. 20141006. Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A. : Human mutation.
Harvard
Soldovieri M. V., Boutry-Kryza N., Milh M., Doummar D., Heron B., Bourel E., Ambrosino P., Miceli F., De Maria M., Dorison N., Auvin S., Echenne B., Oertel J., Riquet A., Lambert L., Gerard M., Roubergue A., Calender A., Mignot C., Taglialatela M. and Lesca G. (20141006). Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A. : Human mutation.
MLA
Soldovieri Maria Virginia, Boutry-Kryza Nadia, Milh Mathieu, Doummar Diane, Heron Benedicte, Bourel Emilie, Ambrosino Paolo, Miceli Francesco, De Maria Michela, Dorison Nathalie, Auvin Stephane, Echenne Bernard, Oertel Julie, Riquet Audrey, Lambert Laetitia, Gerard Marion, Roubergue Anne, Calender Alain, Mignot Cyril, Taglialatela Maurizio and Lesca Gaetan. Novel KCNQ2 and KCNQ3 mutations in a large cohort of families with benign neonatal epilepsy: first evidence for an altered channel regulation by syntaxin-1A. : Human mutation. 20141006.