Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome.

MLA

Aoki, Yoko, et al. “Gain-of-Function Mutations in RIT1 Cause Noonan Syndrome, a RAS/MAPK Pathway Syndrome.” American Journal of Human Genetics, vol. 93, no. 1, July 2013, pp. 173–80. EBSCOhost, https://doi.org/10.1016/j.ajhg.2013.05.021.

APA

Aoki, Y., Niihori, T., Banjo, T., Okamoto, N., Mizuno, S., Kurosawa, K., Ogata, T., Takada, F., Yano, M., Ando, T., Hoshika, T., Barnett, C., Ohashi, H., Kawame, H., Hasegawa, T., Okutani, T., Nagashima, T., Hasegawa, S., Funayama, R., … Matsubara, Y. (2013). Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome. American Journal of Human Genetics, 93(1), 173–180. https://doi.org/10.1016/j.ajhg.2013.05.021

Chicago

Aoki, Yoko, Tetsuya Niihori, Toshihiro Banjo, Nobuhiko Okamoto, Seiji Mizuno, Kenji Kurosawa, Tsutomu Ogata, et al. 2013. “Gain-of-Function Mutations in RIT1 Cause Noonan Syndrome, a RAS/MAPK Pathway Syndrome.” American Journal of Human Genetics 93 (1): 173–80. doi:10.1016/j.ajhg.2013.05.021.