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- W2097510177 abstract "ABSTRACT: End-organ resistance to androgens, called androgen insensitivity syndrome (AIS), is a rare disorder. The most common cause of AIS is mutations(s) in the androgen receptor (AR) gene; however, a significant number of these mutations have not been functionally analyzed. In the present study, we analyzed a case of complete AIS for mutations in the AR gene. Sequencing of the entire coding region of the AR gene revealed a 2650G>A mutation (mRNA sequence reference) in exon 4 of the gene, resulting in replacement of glycine with glutamate at codon 708 in the ligand-binding domain of the AR protein. The mutation was absent in 200 normal male individuals analyzed to look at its occurrence in general population. In vitro androgen-binding and transactivation assays showed that the mutation resulted in approximately 65% loss of ligand binding and almost complete loss of transactivation function. Complete AIS in this individual was due to a G708E substitution in the AR protein." @default.
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- W2097510177 date "2010-07-29" @default.
- W2097510177 modified "2023-10-18" @default.
- W2097510177 title "G708E Mutation in the Androgen Receptor Results in Complete Loss of Androgen Function" @default.
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- W2097510177 doi "https://doi.org/10.2164/jandrol.110.010736" @default.
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