Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination.

MLA

Nakayama, Tojo, et al. “Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination.” American Journal of Human Genetics, vol. 96, no. 5, May 2015, pp. 709–19. EBSCOhost, https://doi.org/10.1016/j.ajhg.2015.03.003.

APA

Nakayama, T., Al-Maawali, A., El-Quessny, M., Rajab, A., Khalil, S., Stoler, J. M., Tan, W.-H., Nasir, R., Schmitz-Abe, K., Hill, R. S., Partlow, J. N., Al-Saffar, M., Servattalab, S., LaCoursiere, C. M., Tambunan, D. E., Coulter, M. E., Elhosary, P. C., Gorski, G., Barkovich, A. J., … Mochida, G. H. (2015). Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination. American Journal of Human Genetics, 96(5), 709–719. https://doi.org/10.1016/j.ajhg.2015.03.003

Chicago

Nakayama, Tojo, Almundher Al-Maawali, Malak El-Quessny, Anna Rajab, Samir Khalil, Joan M Stoler, Wen-Hann Tan, et al. 2015. “Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination.” American Journal of Human Genetics 96 (5): 709–19. doi:10.1016/j.ajhg.2015.03.003.