Extracellular correction of the androgen-receptor transformation defect in two families with complete androgen resistance
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Biochemistry
Reference32 articles.
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1. Correlation between genotype, phenotype and sex of rearing in 111 patients with partial androgen insensitivity syndrome;Clinical Endocrinology;2005-07
2. Bridging structural biology and genetics by computational methods: An investigation into how the R774C mutation in the AR gene can result in complete androgen insensitivity syndrome;Human Mutation;2003-11-17
3. The Use of Androgen Receptor Amino/Carboxyl-Terminal Interaction Assays to Investigate Androgen Receptor Gene Mutations in Subjects with Varying Degrees of Androgen Insensitivity;The Journal of Clinical Endocrinology & Metabolism;2003-05
4. Molecular basis of androgen receptor diseases;Annals of Medicine;2000-01
5. Oligospermic infertility associated with an androgen receptor mutation that disrupts interdomain and coactivator (TIF2) interactions;Journal of Clinical Investigation;1999-06-01
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