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Complete androgen insensitivity syndrome caused by the c.2678C>T mutation in the androgen receptor gene: A case report
BACKGROUND: Androgen insensitivity syndrome is an X-linked recessive genetic disease caused by mutations in the androgen receptor gene (AR). However, the underlying molecular mechanisms for the majority of AR variants remain unclear. In this study, we identified a point variant in three patients wit...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Baishideng Publishing Group Inc
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8678886/ https://www.ncbi.nlm.nih.gov/pubmed/35047615 http://dx.doi.org/10.12998/wjcc.v9.i35.11036 |