Audo, I., Bujakowska, K., Orhan, E., Poloschek, C., Defoort-Dhellemmes, S., Drumare, I., . . . Zeitz, C. (2012). Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness. Elsevier.
Citación estilo ChicagoAudo, Isabelle, et al. Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness. Elsevier, 2012.
Cita MLAAudo, Isabelle, et al. Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness. Elsevier, 2012.
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