Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR Activity

CONTEXT: Only approximately 85% of patients with a clinical diagnosis complete androgen insensitivity syndrome and less than 30% with partial androgen insensitivity syndrome can be explained by inactivating mutations in the androgen receptor (AR) gene. OBJECTIVE: The objective of the study was to cl...

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Detalles Bibliográficos
Autores principales: Hornig, N. C., Ukat, M., Schweikert, H. U., Hiort, O., Werner, R., Drop, S. L. S., Cools, M., Hughes, I. A., Audi, L., Ahmed, S. F., Demiri, J., Rodens, P., Worch, L., Wehner, G., Kulle, A. E., Dunstheimer, D., Müller-Roßberg, E., Reinehr, T., Hadidi, A. T., Eckstein, A. K., van der Horst, C., Seif, C., Siebert, R., Ammerpohl, O., Holterhus, P.-M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2016
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095254/
https://www.ncbi.nlm.nih.gov/pubmed/27583472
http://dx.doi.org/10.1210/jc.2016-1990

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095254/
https://www.ncbi.nlm.nih.gov/pubmed/27583472
http://dx.doi.org/10.1210/jc.2016-1990

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