APA
Milh M., Boutry-Kryza N., Sutera-Sardo J., Mignot C., Auvin S., Lacoste C., Villeneuve N., Roubertie A., Heron B., Carneiro M., Kaminska A., Altuzarra C., Blanchard G., Ville D., Barthez M. A., Heron D., Gras D., Afenjar A., Dorison N., Doummar D., Billette de Villemeur T., An I., Jacquette A., Charles P., Perrier J., Isidor B., Vercueil L., Chabrol B., Badens C., Lesca G. & Villard L. (20140102). Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2. : Orphanet journal of rare diseases.
Chicago
Milh Mathieu, Boutry-Kryza Nadia, Sutera-Sardo Julie, Mignot Cyril, Auvin Stéphane, Lacoste Caroline, Villeneuve Nathalie, Roubertie Agathe, Heron Bénédicte, Carneiro Maryline, Kaminska Anna, Altuzarra Cécilia, Blanchard Gaëlle, Ville Dorothée, Barthez Marie Anne, Heron Delphine, Gras Domitille, Afenjar Alexandra, Dorison Nathalie, Doummar Dianne, Billette de Villemeur Thierry, An Isabelle, Jacquette Aurélia, Charles Perrine, Perrier Julie, Isidor Bertrand, Vercueil Laurent, Chabrol Brigitte, Badens Catherine, Lesca Gaétan and Villard Laurent. 20140102. Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2. : Orphanet journal of rare diseases.
Harvard
Milh M., Boutry-Kryza N., Sutera-Sardo J., Mignot C., Auvin S., Lacoste C., Villeneuve N., Roubertie A., Heron B., Carneiro M., Kaminska A., Altuzarra C., Blanchard G., Ville D., Barthez M. A., Heron D., Gras D., Afenjar A., Dorison N., Doummar D., Billette de Villemeur T., An I., Jacquette A., Charles P., Perrier J., Isidor B., Vercueil L., Chabrol B., Badens C., Lesca G. and Villard L. (20140102). Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2. : Orphanet journal of rare diseases.
MLA
Milh Mathieu, Boutry-Kryza Nadia, Sutera-Sardo Julie, Mignot Cyril, Auvin Stéphane, Lacoste Caroline, Villeneuve Nathalie, Roubertie Agathe, Heron Bénédicte, Carneiro Maryline, Kaminska Anna, Altuzarra Cécilia, Blanchard Gaëlle, Ville Dorothée, Barthez Marie Anne, Heron Delphine, Gras Domitille, Afenjar Alexandra, Dorison Nathalie, Doummar Dianne, Billette de Villemeur Thierry, An Isabelle, Jacquette Aurélia, Charles Perrine, Perrier Julie, Isidor Bertrand, Vercueil Laurent, Chabrol Brigitte, Badens Catherine, Lesca Gaétan and Villard Laurent. Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2. : Orphanet journal of rare diseases. 20140102.