Cite
Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism.
MLA
Masaki Takagi, et al. “Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients with Congenital Hypopituitarism.” PLoS ONE, vol. 7, no. 9, Jan. 2012, p. e46008. EBSCOhost, https://doi.org/10.1371/journal.pone.0046008.
APA
Masaki Takagi, Tomohiro Ishii, Mikako Inokuchi, Naoko Amano, Satoshi Narumi, Yumi Asakura, Koji Muroya, Yukihiro Hasegawa, Masanori Adachi, & Tomonobu Hasegawa. (2012). Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism. PLoS ONE, 7(9), e46008. https://doi.org/10.1371/journal.pone.0046008
Chicago
Masaki Takagi, Tomohiro Ishii, Mikako Inokuchi, Naoko Amano, Satoshi Narumi, Yumi Asakura, Koji Muroya, Yukihiro Hasegawa, Masanori Adachi, and Tomonobu Hasegawa. 2012. “Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients with Congenital Hypopituitarism.” PLoS ONE 7 (9): e46008. doi:10.1371/journal.pone.0046008.