Structural characterization of normal and mutant human steroid 17α-hydroxylase genes: molecular basis of one example of combined 17α-hydroxylase/17,20 lyase deficiencyKAGIMOTO, M; WINTER, J. S. D; KAGIMOTO, K et al.Molecular endocrinology (Baltimore, Md.). 1988, Vol 2, Num 6, pp 564-570, issn 0888-8809Article

A NEW ASSAY AND SOLUBILIZATION PROCEDURE FOR STEROID 17,20-LYASE FROM RAT TESTESCHASALOW FI; MARR H; TAYLOR G et al.1982; STEROIDS; ISSN 0039-128X; USA; DA. 1982; VOL. 39; NO 6; PP. 617-630; BIBL. 18 REF.Article

18q Deletion syndrome in a child with steroid-17,20-lyase deficiencyCHASALOW, F. I; BLETHEN, S. L; KNIGHT, S. M et al.Steroids. 1986, Vol 47, Num 6, pp 421-429, issn 0039-128XArticle

Molecular basis of 17α-hydroxylase/17,20-lyase deficiencyYANASE, T; IMAI, T; SIMPSON, E. R et al.Journal of steroid biochemistry and molecular biology. 1992, Vol 43, Num 8, pp 973-979, issn 0960-0760Conference Paper

Mutation R96W in cytochrome P450c17 gene causes combined 17α-hydroxylase/17-20-lyase deficiency in two French Canadian patientsLAFLAMME, N; LEBLANC, J.-F; MAILLOUX, J et al.The Journal of clinical endocrinology and metabolism. 1996, Vol 81, Num 1, pp 264-268, issn 0021-972XArticle

The genetic and functional basis of isolated 17,20-lyase deficiencyGELLER, D. H; AUCHUS, R. J; MENDONCA, B. B et al.Nature genetics. 1997, Vol 17, Num 2, pp 201-205, issn 1061-4036Article