Ruiter, P. de

reductase androgen subject reductase 2 gene mutation sibling receptor expression activity reductase 2 activity reductase 2 deficiency subject ii patient skin fibroblasts phenotypic ar gene deficiency androgen receptor androgen insensitivity syndrome library erasmus mc analysis level phenotype endocrinol fibroblast variation binding reductase activity insensitivity family serum gsf cell lines range reductase 2 expression srd 5a gene reductase deficiency subject ii -8 control difference russell dw wilson jd syndrome phenotypic variation wilson protein intron sequences androgen insensitivity reductase 2 114 kda reductase 2- hormone metab defect testosterone november shbg serum level sequence m 2001 vol phosphorylation ar gene mutation urogenital suppression labia minora endocrinology isoform erasmu wild-type cells study reaction ii -8 r 846h mol endocrinol cell lines hughes ia exon 1 enzyme boehmer downloaded library biopsy