Human androgen insensitivity due to point mutations encoding amino acid substitutions in the androgen receptor steroid-binding domain
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference34 articles.
1. A single-base substitution in exon 6 of the androgen receptor gene causing complete androgen insensitivity: the mutated receptor fails to transactivate but binds to DNA in vitro
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1. Rare Case of Complete Androgen Insensitivity Syndrome;Cureus;2024-02-20
2. A hotspot for posttranslational modifications on the androgen receptor dimer interface drives pathology and anti-androgen resistance;Science Advances;2023-03-17
3. A hemizygous mutation in the androgen receptor gene causes different phenotypes of androgen insensitivity syndrome in two siblings by disrupting the nuclear translocation;Molecular Genetics and Genomics;2020-05-20
4. Phenotypic and molecular characteristics of androgen insensitivity syndrome patients;Asian Journal of Andrology;2018
5. Structure of the homodimeric androgen receptor ligand-binding domain;Nature Communications;2017-02-06
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