NPHP3 mutations are associated with neonatal onset multiorgan polycystic disease in two siblings.

MLA

Leeman, K. T., et al. “NPHP3 Mutations Are Associated with Neonatal Onset Multiorgan Polycystic Disease in Two Siblings.” Journal of Perinatology : Official Journal of the California Perinatal Association, vol. 34, no. 5, May 2014, pp. 410–11. EBSCOhost, https://doi.org/10.1038/jp.2014.20.

APA

Leeman, K. T., Dobson, L., Towne, M., Dukhovny, D., Joshi, M., Stoler, J., & Agrawal, P. B. (2014). NPHP3 mutations are associated with neonatal onset multiorgan polycystic disease in two siblings. Journal of Perinatology : Official Journal of the California Perinatal Association, 34(5), 410–411. https://doi.org/10.1038/jp.2014.20

Chicago

Leeman, K T, L Dobson, M Towne, D Dukhovny, M Joshi, J Stoler, and P B Agrawal. 2014. “NPHP3 Mutations Are Associated with Neonatal Onset Multiorgan Polycystic Disease in Two Siblings.” Journal of Perinatology : Official Journal of the California Perinatal Association 34 (5): 410–11. doi:10.1038/jp.2014.20.