1. Ahlgren, R., Yanase, T., Simpson, E. R., Winter, J. S., & Waterman, M. R. (1992). Compound heterozygous mutations (Arg 239—stop, Pro 342—Thr) in the CYP17 (P45017 alpha) gene lead to ambiguous external genitalia in a male patient with partial combined 17 alpha-hydroxylase/17, 20-lyase deficiency. Journal of Clinical Endocrinology and Metabolism, 74, 667–672.
2. Arlt, W., Martens, J. W., Song, M., Wang, J. T., Auchus, R. J., & Miller, W. L. (2002). Molecular evolution of adrenarche: structural and functional analysis of p450c17 from four primate species. Endocrinology, 143, 4665–4672.
3. Auchus, R. J., & Miller, W. L. (1999). Molecular modeling of human P450c17 (17alpha-hydroxylase/17, 20-lyase): insights into reaction mechanisms and effects of mutations. Molecular Endocrinology, 13, 1169–1182.
4. Auchus, R. J., Lee, T. C., & Miller, W. L. (1998). Cytochrome b5 augments the 17, 20-lyase activity of human P450c17 without direct electron transfer. The Journal of Biological Chemistry, 273, 3158–3165.
5. Baker, M. E. (2001). Evolution of 17beta-hydroxysteroid dehydrogenases and their role in androgen, estrogen and retinoid action. Molecular and Cellular Endocrinology, 171, 211–215.