Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction.

MLA

Roosing, Susanne, et al. “Maternal Uniparental Isodisomy of Chromosome 6 Reveals a TULP1 Mutation as a Novel Cause of Cone Dysfunction.” Ophthalmology, vol. 120, no. 6, June 2013, pp. 1239–46. EBSCOhost, https://doi.org/10.1016/j.ophtha.2012.12.005.

APA

Roosing, S., van den Born, L. I., Hoyng, C. B., Thiadens, A. A. H. J., de Baere, E., Collin, R. W. J., Koenekoop, R. K., Leroy, B. P., van Moll-Ramirez, N., Venselaar, H., Riemslag, F. C. C., Cremers, F. P. M., Klaver, C. C. W., & den Hollander, A. I. (2013). Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction. Ophthalmology, 120(6), 1239–1246. https://doi.org/10.1016/j.ophtha.2012.12.005

Chicago

Roosing, Susanne, L Ingeborgh van den Born, Carel B Hoyng, Alberta A H J Thiadens, Elfride de Baere, Rob W J Collin, Robert K Koenekoop, et al. 2013. “Maternal Uniparental Isodisomy of Chromosome 6 Reveals a TULP1 Mutation as a Novel Cause of Cone Dysfunction.” Ophthalmology 120 (6): 1239–46. doi:10.1016/j.ophtha.2012.12.005.