Cita APA (7a ed.)
Zeitz, C., Méjécase, C., Stévenard, M., Michiels, C., Audo, I., & Marmor, M. F. (2018). A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness. BioMed Research International, 2018, 1-11.
Cita Chicago Style (17a ed.)
Zeitz, Christina, Cécile Méjécase, Mathilde Stévenard, Christelle Michiels, Isabelle Audo, y Michael F. Marmor. "A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness." BioMed Research International 2018 (2018): 1-11.
Cita MLA (9a ed.)
Zeitz, Christina, et al. "A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness." BioMed Research International, vol. 2018, 2018, pp. 1-11.
Precaución: Estas citas no son 100% exactas.