7 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 12706306 | A complex heterozygous mutation of His373Leu and Asp487-Ser488-Phe489 deletion in human cytochrome P450c17 causes 17alpha-hydroxylase/17,20-lyase deficiency in three Chinese sisters. | 2003 Mar 28 | 1 |
2 | 11836339 | Combined 17alpha-Hydroxylase/17,20-lyase deficiency caused by Phe93Cys mutation in the CYP17 gene. | 2002 Feb | 1 |
3 | 10620365 | The use of random chimeragenesis to study structure/function properties of rat and human P450c17. | 2000 Jan 15 | 1 |
4 | 10856480 | Induction of endometrial cycles and ovulation in a woman with combined 17alpha-hydroxylase/17,20-lyase deficiency due to compound heterozygous mutations on the p45017alpha gene. | 2000 Jun | 1 |
5 | 8855840 | Mutation of cytochrome P-45017 alpha gene (CYP17) in a Japanese patient previously reported as having glucocorticoid-responsive hyperaldosteronism: with a review of Japanese patients with mutations of CYP17. | 1996 Oct | 2 |
6 | 8345056 | Deletion of amino acids Asp487-Ser488-Phe489 in human cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency. | 1993 Aug | 1 |
7 | 2808364 | Deletion of a phenylalanine in the N-terminal region of human cytochrome P-450(17 alpha) results in partial combined 17 alpha-hydroxylase/17,20-lyase deficiency. | 1989 Oct 25 | 1 |