Phenotypic and molecular characteristics of androgen insensitivity syndrome patients

Androgen insensitivity syndrome (AIS), an X-linked recessive genetic disorder of sex development, is caused by mutations in the androgen receptor (AR) gene, and is characterized by partial or complete inability of specific tissues to respond to androgens in individuals with the 46, XY karyotype. Thi...

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Detalles Bibliográficos
Autores principales: Yuan, Shi-Min, Zhang, Ya-Nan, Du, Juan, Li, Wen, Tu, Chao-Feng, Meng, Lan-Lan, Lin, Ge, Lu, Guang-Xiu, Tan, Yue-Qiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116692/
https://www.ncbi.nlm.nih.gov/pubmed/29785970
http://dx.doi.org/10.4103/aja.aja_17_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116692/
https://www.ncbi.nlm.nih.gov/pubmed/29785970
http://dx.doi.org/10.4103/aja.aja_17_18

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