Associated Papers
Characterization of a novel androgen receptor gene variant identified in an Iranian family with complete androgen insensitivity syndrome (CAIS): a molecular dynamics simulation study.
Aghaei S et al.
Journal of Biomolecular Structure & Dynamics, 2023
A hemizygous mutation in the androgen receptor gene causes different phenotypes of androgen insensitivity syndrome in two siblings by disrupting the nuclear translocation.
Liu C et al.
Molecular Genetics and Genomics : Mgg, 2020
Phenotypic and molecular characteristics of androgen insensitivity syndrome patients.
Yuan SM et al.
Asian Journal of Andrology, 0
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