Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2.

MLA

Milh, Mathieu, et al. “Similar Early Characteristics but Variable Neurological Outcome of Patients with a de Novo Mutation of KCNQ2.” Orphanet Journal of Rare Diseases, vol. 8, May 2013, p. 80. EBSCOhost, https://doi.org/10.1186/1750-1172-8-80.

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., … Villard, L. (2013). Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2. Orphanet Journal of Rare Diseases, 8, 80. https://doi.org/10.1186/1750-1172-8-80

Chicago

Milh, Mathieu, Nadia Boutry-Kryza, Julie Sutera-Sardo, Cyril Mignot, Stéphane Auvin, Caroline Lacoste, Nathalie Villeneuve, et al. 2013. “Similar Early Characteristics but Variable Neurological Outcome of Patients with a de Novo Mutation of KCNQ2.” Orphanet Journal of Rare Diseases 8 (May): 80. doi:10.1186/1750-1172-8-80.