APA Alıntı

Sakoh, T., Sekine, A., Mori, T., Mizuno, H., Kawada, M., Hiramatsu, R., . . . Takaichi, K. (2019). A familial case of pseudohypoaldosteronism type II (PHA2) with a novel mutation (D564N) in the acidic motif in WNK4. Mol Genet Genomic Med.

Chicago Stili Alıntı

Sakoh, Takashi, et al. "A Familial Case of Pseudohypoaldosteronism Type II (PHA2) With a Novel Mutation (D564N) in the Acidic Motif in WNK4." Mol Genet Genomic Med 2019.

MLA Alıntı

Sakoh, Takashi, et al. "A Familial Case of Pseudohypoaldosteronism Type II (PHA2) With a Novel Mutation (D564N) in the Acidic Motif in WNK4." Mol Genet Genomic Med 2019.