Nonsense pathogenic variants in exon 1 of PHOX2B lead to translational reinitiation in congenital central hypoventilation syndrome.

MLA

Cain, Jacob T., et al. “Nonsense Pathogenic Variants in Exon 1 of PHOX2B Lead to Translational Reinitiation in Congenital Central Hypoventilation Syndrome.” American Journal of Medical Genetics. Part A, vol. 173, no. 5, May 2017, pp. 1200–07. EBSCOhost, https://doi.org/10.1002/ajmg.a.38162.

APA

Cain, J. T., Kim, D. I., Quast, M., Shivega, W. G., Patrick, R. J., Moser, C., Reuter, S., Perez, M., Myers, A., Weimer, J. M., Roux, K. J., & Landsverk, M. (2017). Nonsense pathogenic variants in exon 1 of PHOX2B lead to translational reinitiation in congenital central hypoventilation syndrome. American Journal of Medical Genetics. Part A, 173(5), 1200–1207. https://doi.org/10.1002/ajmg.a.38162

Chicago

Cain, Jacob T, Dae I Kim, Megan Quast, Winnie G Shivega, Ryan J Patrick, Chuanpit Moser, Suzanne Reuter, et al. 2017. “Nonsense Pathogenic Variants in Exon 1 of PHOX2B Lead to Translational Reinitiation in Congenital Central Hypoventilation Syndrome.” American Journal of Medical Genetics. Part A 173 (5): 1200–1207. doi:10.1002/ajmg.a.38162.