Associated Papers
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
Systematic and functional characterization of novel androgen receptor variants arising from alternative splicing in the ligand-binding domain.
Uo T et al.
Oncogene, 2017
Phenotypic and molecular characteristics of androgen insensitivity syndrome patients.
Yuan SM et al.
Asian Journal of Andrology, 0
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