Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiency.

MLA

Penhoat, A., et al. “Functional Relationships between Three Novel Homozygous Mutations in the ACTH Receptor Gene and Familial Glucocorticoid Deficiency.” Journal of Molecular Medicine (Berlin, Germany), vol. 80, no. 7, July 2002, pp. 406–11. EBSCOhost, https://doi.org/10.1007/s00109-002-0333-7.

APA

Penhoat, A., Naville, D., El Mourabit, H., Buronfosse, A., Berberoglu, M., Ocal, G., Tsigos, C., Durand, P., & Bégeot, M. (2002). Functional relationships between three novel homozygous mutations in the ACTH receptor gene and familial glucocorticoid deficiency. Journal of Molecular Medicine (Berlin, Germany), 80(7), 406–411. https://doi.org/10.1007/s00109-002-0333-7

Chicago

Penhoat, A, D Naville, H El Mourabit, A Buronfosse, M Berberoglu, G Ocal, C Tsigos, P Durand, and M Bégeot. 2002. “Functional Relationships between Three Novel Homozygous Mutations in the ACTH Receptor Gene and Familial Glucocorticoid Deficiency.” Journal of Molecular Medicine (Berlin, Germany) 80 (7): 406–11. doi:10.1007/s00109-002-0333-7.