Ontology highlight
ABSTRACT:
SUBMITTER: Tyutyusheva N
PROVIDER: S-EPMC7865707 | biostudies-literature | 2021 Jan
REPOSITORIES: biostudies-literature
Tyutyusheva Nina N Mancini Ilaria I Baroncelli Giampiero Igli GI D'Elios Sofia S Peroni Diego D Meriggiola Maria Cristina MC Bertelloni Silvano S
International journal of molecular sciences 20210127 3
Complete androgen insensitivity syndrome (CAIS) is due to complete resistance to the action of androgens, determining a female phenotype in persons with a 46,XY karyotype and functioning testes. CAIS is caused by inactivating mutations in the androgen receptor gene (<i>AR</i>). It is organized in eight exons located on the X chromosome. Hundreds of genetic variants in the <i>AR</i> gene have been reported in CAIS. They are distributed throughout the gene with a preponderance located in the ligan ...[more]