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...

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Detalles Bibliográficos
Autores principales: Wang, Ka-Na, Chen, Qing-Qing, Zhu, Yi-Lin, Wang, Chun-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2021
Materias:
Case Report
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

Internet

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

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