Méjécase, C., Laurent-Coriat, C., Mayer, C., Poch, O., Mohand-Saïd, S., Prévot, C., . . . Zeitz, C. (2016). Identification of a Novel Homozygous Nonsense Mutation Confirms the Implication of GNAT1 in Rod-Cone Dystrophy. PLoS One.
Chicago Style CitationMéjécase, Cécile, et al. "Identification of a Novel Homozygous Nonsense Mutation Confirms the Implication of GNAT1 in Rod-Cone Dystrophy." PLoS One 2016.
MLA CitationMéjécase, Cécile, et al. "Identification of a Novel Homozygous Nonsense Mutation Confirms the Implication of GNAT1 in Rod-Cone Dystrophy." PLoS One 2016.
Warning: These citations may not always be 100% accurate.