Identification of a homozygous c.1039C>T (p.R347C) variant in CYP17A1 in a 67-year-old female patient with partial 17α-hydroxylase/17,20-lyase deficiency.

MLA

Satoshi Yamagata, et al. “Identification of a Homozygous c.1039C>T (p.R347C) Variant in CYP17A1 in a 67-Year-Old Female Patient with Partial 17α-Hydroxylase/17,20-Lyase Deficiency.” Endocrine Journal, vol. 69, no. 2, Feb. 2022, pp. 115–20. EBSCOhost, https://doi.org/10.1507/endocrj.ej21-0266.

APA

Satoshi Yamagata, Kazunori Kageyama, Takeshi Usui, Kohei Saito, Shinobu Takayasu, Mari Usutani, Ken Terui, & Makoto Daimon. (2022). Identification of a homozygous c.1039C>T (p.R347C) variant in CYP17A1 in a 67-year-old female patient with partial 17α-hydroxylase/17,20-lyase deficiency. Endocrine Journal, 69(2), 115–120. https://doi.org/10.1507/endocrj.ej21-0266

Chicago

Satoshi Yamagata, Kazunori Kageyama, Takeshi Usui, Kohei Saito, Shinobu Takayasu, Mari Usutani, Ken Terui, and Makoto Daimon. 2022. “Identification of a Homozygous c.1039C>T (p.R347C) Variant in CYP17A1 in a 67-Year-Old Female Patient with Partial 17α-Hydroxylase/17,20-Lyase Deficiency.” Endocrine Journal 69 (2): 115–20. doi:10.1507/endocrj.ej21-0266.